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Esoteric Departments: All Available Tests

RBC Special Studies View Department Homepage

TESTS:
Select a test to view Test Description & Clinical Indications
TEST CODES:
Select a Test Code to view Test Specimen Collection Instructions
ADENOSINE DEAMINASE (ADA), BLOOD, QUANTITATIVE ADAQ
EMA (EOSIN-5-MALEIMIDE) BY FLOW CYTOMETRY EMA
G6PD FEMALE CARRIER STATUS PANEL LABG6PDF
GLUCOSE-6-PHOSPHATE DEHYDROGENASE, QUANTITATIVE, WHOLE BLOOD G6PDQT
HEMOGLOBIN F QUANTITATIVE HGBFQ
HEMOGLOBIN QUANTITATION / FRACTIONATION BY CAPILLARY ZONE ELECTROPHORESIS HGBQ
HEMOGLOBIN S QUANTITATIVE HGBSQ
OSMOTIC FRAGILITY, RBC OF
PURINE NUCLEOSIDE PHOSPHORYLASE (PNP) QUANTITATIVE PNPQ
RBC ENZYME PANEL RBCENZ

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Biochemical Genetics View Department Homepage

TESTS: Select a test to view Test Description & Clinical IndicationsTEST CODES:
Select a Test Code to view Test Specimen Collection Instructions
ACYLCARNITINE PROFILE, QUANTITATIVEACYLP
AMINO ACIDS, BLOOD SPOTAABS
AMINO ACIDS, QUANTITATIVE, CSFAACSF
AMINO ACIDS, QUANTITATIVE, PLASMAAAP
AMINO ACIDS, QUANTITATIVE, URINEAAUR
BIOTINIDASEBTDASE
CARNITINE, FREE AND TOTAL, PLASMA/SERUMCARN
CARNITINE, FREE AND TOTAL, URINEUCARN
GLUTATHIONE, WHOLE BLOODLAB274
METHYLMALONIC ACID, SERUMMMAS
MUCOPOLYSACCHARIDES, TLC, URINEMPSTLC
MUCOPOLYSACCHARIDES, URINE, QUANTITATIVEMPSQNT
OLIGOSACCHARIDES, QUALITATIVE BY MASS SPECTROMETRY, URINEOSLCMS
ORGANIC ACIDS, QUALITATIVE, URINEUORG
OROTIC ACID, URINEUOROT

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Cytogenetics/FISH View Department Homepage

TESTS:
Select a test to view Test Description & Clinical Indications
TEST CODES:
Select a Test Code to view Test Specimen Collection Instructions
12P COPY NUMBER FISH 12Pcn
13Q, FISH CGFi 13Q
1P/19Q DELETIONS IN OLIGODENDROGLIOMA FISH GLIOMA
5Q, FISH CGFi 5Q
7Q, FISH CGFi 7Q
ALK GENE REARRANGEMENT FISH ALK
ALK, FISH CGFi ALK
ANGELMAN SYNDROME (AS), 15Q11.2 (D15S10 DELETION) CGF ANGLM
ARRAY COMPARATIVE GENOMIC HYBRIDIZATION (ACGH) CGH GEN
BCL2 GENE REARRANGEMENT (CG FISH) CGFi BCL2
BCL2 GENE REARRANGEMENT IN FOLLICULAR LYMPHOMA (FISH BCL2 ) FISH BCL2
BCL6, FISH CGFi BCL6
BCR/ABL GENE FUSION IN CML AND ALL, T(9;22)(Q34;Q11.2) CGFi BCR
BLADDER CANCER FISH, UROVYSION CGFi UROV
BRAF GENE REARRANGEMENT FISH BRAF
CCND1 GENE REARRANGEMENT (FFPE) FISH CCND1
CCND1/IGH, FISH CGFi t(11;14)
CENTROMERE PROBES (CROSS SEX TRANSPLANT; ANAUPLOIDY) CGFi ENUM
CHROM. #1 COPY NUMBER CGFi 1Q1P
CLL PANEL (+12, 11Q AND 13Q DELETION, 17P DELETION) [PERIPHERAL BLOOD PREFERRED] CGFi CLL
CRLF2, FISH CGFi CRLF2
CYTOGENETIC STUDY - AMNIOTIC FLUID CG AMNIO
CYTOGENETIC STUDY, BLOOD (CANCER DX.) CG BLD NEO
CYTOGENETIC STUDY, BLOOD, HIGH RESOLUTION CG HI RES
CYTOGENETIC STUDY, BLOOD, ROUTINE / PERCUTANEOUS UMBILICAL BLOOD SAMPLING (PUBS) CG BLOOD
CYTOGENETIC STUDY, BONE MARROW CG BONE MRW
CYTOGENETIC STUDY, CHORIONIC VILLI CG CVS
CYTOGENETIC STUDY, CHROMOSOME BREAKAGE FOR FANCONI ANEMIA CG FANCONI
CYTOGENETIC STUDY, TISSUE, POC CG TISS POC
CYTOGENETIC STUDY, TISSUE, SKIN/OTHER CG TISS SKIN
CYTOGENETIC STUDY, TUMOR CG TUMOR
DIGEORGE SEQUENCE/VELOCARDIOFACIAL SYNDROME (VCF), 22Q11.2 (TUPLE1 DELETION) AND DISTAL 22Q13.3 DELETION (ARSA) CGF VCF
EGFR GENE AMPLIFICATION FISH EGFR
ETV6 GENE REARRANGEMENT FISH ETV6
ETV6, FISH CGFi ETV6
ETV6/RUNX1, FISH CGFi TEL
EWSR1 GENE REARRANGEMENT FISH EWSR1
FGFR1, FISH CGFi FGFR1
FISH CHIC2 CGFi CHIC2
FOXO1 GENE REARRANGEMENT IN ALVEOLAR RHABDOMYOSARCOMA FISH FOXO1
FOXO1, FISH CGFi FOXO1
FUS GENE REARRANGEMENT FISH FUS
HER2 AMPLIFICATION FISH HER2
HER2 GENE AMPLIFICATION, NON-BREAST FISH HER2nb
IGH FISH CGFi IGH
IGH/BCL2, FISH CGFi t(14;18)
IGH/FGFR3, FISH CGFi t(4;14)
IGH/MAF, FISH CGFi t(14;16)
INV(16) FISH CGFi inv(16)
KRAS GENE AMPLIFICATION FISH KRAS
MAML2 GENE REARRANGEMENT FISH MAML2
MDM2 GENE AMPLIFICATION FISH MDM2
MDS PANEL, FISH CGFi MDSpan
MET GENE AMPLIFICATION FISH METamp
MILLER-DIEKER SYNDROME (MDS), 17P13.3 (LIS1 DELETION) CGF MDK
MLL, FISH CGFi MLL
MYB GENE REARRANGEMENT FISH MYB
MYC GENE REARRANGEMENT IN BURKITT, OTHER LYMPHOMA FISH MYC
MYC, FISH CGFi MYC
MYELOMA PANEL, FISH CGFi MMpan
P53, FISH CGFi P53
PDGFRB GENE REARRANGEMENT CGFi PDGRFB
PLAG1 GENE REARRANGEMENT FISH PLAG1
PML/RARA GENE FUSION IN APL, T(15;17)(Q22;Q21) CGFi APL
PRADER-WILLI SYNDROME (PWS), 15Q11.2 (SNRPN DELETION) CGF PWS
PRENATAL SCREEN, FISH CGF PRENAT
PRKACA GENE REARRANGEMENT FISH PRKACA
ROS1 GENE REARRANGEMENT FISH ROS1
RUNX1T1/RUNX1, FISH CGFi t(8;21)
SMITH-MAGENIS SYNDROME (SMS), 17P11.2 (FL1 DELETION) CGF SMS
SS18 (SYT) GENE REARRANGEMENT FISH SS18
TFE3 GENE REARRANGEMENT FISH TFE3
TRISOMY 8 CGFi ENUM
WILLIAMS SYNDROME (WS), 7Q11.23 (WSCR DELETION) CGF WMS

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Virology View Department Homepage

TESTS:
Select a test to view Test Description & Clinical Indications
TEST CODES:
Select a Test Code to view Test Specimen Collection Instructions
ADENOVIRUS QUANTITATIVE PCR, PLASMA ORDER ADVQT
BK VIRUS DNA PCR PLASMA, QUANTITATIVE BKVPC
BK VIRUS DNA PCR URINE, QUANTITATIVE BKVPCU
CHLAMYDIA TRACHOMATIS AND NEISSERIA GONORRHOEAE (GC), NUCLIEC ACID AMPLIFICATION TESTING (NAAT) CLGC3
CYTOMEGALOVIRUS QUANTITATIVE (CMV VIRAL LOAD) PCR CMVQT
CYTOMEGALOVIRUS(CMV) DNA, QUALITATIVE PCR, NON-PLASMA CMVQL
EPSTEIN BARR VIRUS (EBV) QUANTITATIVE PCR, PLASMA EBVQP
HEPATITIS B PCR QUANTITATIVE, SERUM HBPCR
HEPATITIS C VIRUS (HCV) RNA, QUANTITATIVE PCR, SERUM, WITH REFLEX TO GENOTYPING HCVPCX
HHV-6 QUANTITATIVE PCR, PLASMA ORDER HHV6QT
HIV-1 ANTIVIRAL RESISTANCE TESTING - INTEGRASE AVIN
HIV-1 ANTIVIRAL RESISTANCE TESTING, PROTEASE AND REVERSE-TRANSCRIPTASE, PLASMA AVRT
HIV-1 RNA, QUANTITATIVE PCR, PLASMA HIVPCR
HPV 16/18 TYPING HPVPCR
HPV 6/11 TYPING HPV6PC
HUMAN PAPILLOMAVIRUS VIRUS (HPV), NUCLIEC ACID AMPLIFICATION TESTING (NAAT) HPVHR3

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Molecular Genetic Pathology View Department Homepage

TESTS:
Select a test to view Test Description & Clinical Indications
TEST CODES:
Select a Test Code to view Test Specimen Collection Instructions
A/HYPOCHONDROPLASIA, BLOODCHON
A/HYPOCHONDROPLASIA, NON-BLOODFCHON
ALPHA THALASSEMIA, BLOODATHAL
ALPHA THALASSEMIA, NON-BLOODFATHAL
AML PROGNOSIS ASSAY, BLOODAMLP
AML PROGNOSIS ASSAY, NON-BLOODBMAML
B-CELL CLONALITY BY PCR ,BLOODBCLON
B-CELL CLONALITY, NON-BLOODBMBCLO
BCR-ABL KINASE DOMAIN MUTATION ANALYSIS, BLOODBCRKDM
BCR-ABL KINASE DOMAIN MUTATION ANALYSIS, NON-BLOODNBCRKDM
BCR-ABL, BLOODBCRQT
BCR-ABL, NON-BLOODBMBCRQ
BETA THALASSEMIA SEQUENCING, BLOODBTHSQ
BETA THALASSEMIA SEQUENCING, NON-BLOODFBTHSQ
BIOTINIDASE SEQUENCING ASSAYBIOSA
BRAF, BLOODBRAF
BRAF, NON-BLOODNBRAF
CALRETICULIN MUTATION DETECTION, BLOODCALR
CALRETICULIN MUTATION DETECTION, NON-BLOODNCALR
CDH1 BY SEQUENCING (FAMILIAL GASTRIC CANCER)CDH1
CDH1 MLPA, BLOODCDMLPA
CEBPA, BLOODCEBPA
CEBPA, NON-BLOODBMCEBP
CF POLY-T ANALYSIS, BLOODCFPT
CF POLY-T ANALYSIS, NON-BLOODNCFPT
CFTR DELETION/DUPLICATION ANALYSIS BY MLPACFMLPA
CFTR SCREEN BY SEQUENCINGCFSS
CONNEXIN 26 SEQUENCING, BLOODCX26S
CONNEXIN 26 SEQUENCING, NON-BLOODFCX26S
CONNEXIN 30, BLOODCX30
CONNEXIN 30, NON-BLOODNCX30
CYSTIC FIBROSIS DIAGNOSTIC SEQUENCING ASSAY, BLOODCFDS
CYSTIC FIBROSIS DIAGNOSTIC SEQUENCING ASSAY, NON-BLOODNCFDS
CYSTIC FIBROSIS MUTATION STUDY (CF), BLOODCF32
CYSTIC FIBROSIS MUTATION STUDY (CF), NON BLOODNCF32
DUCHENNE AND BECKER MUSCULAR DYSTROPHIES BY MLPADBMLPA
EGFR, BLOODEGFR
EGFR, NON-BLOODNEGFR
FACTOR V LEIDEN, BLOODLEID
FGFR1 CRANIOSYNOSTOSIS, BLOODFGFR1
FGFR1 CRANIOSYNOSTOSIS, NON-BLOODFFGFR1
FGFR2 CRANIOSYNOSTOSIS, BLOODFGFR2
FGFR2 CRANIOSYNOSTOSIS, NON-BLOODFFGFR2
FGFR3 MUENKE, BLOODFGFR3
FGFR3 MUENKE, NON-BLOODFFGFR3
FRAGILE XFRAGX
HEME-STAMP (STANFORD ACTIONABLE MUTATION PANEL FOR HEMATOPOIETIC AND LYMPHOID NEOPLASMS)LABHSTAMP
HEMOCHROMATOSIS GENOTYPING ASSAYHCHGA
HUNTINGTON'S DISEASE ANALYSIS BY PCRHUNT
IDH1 AND IDH2 MUTATION ANALYSISLABIDH
JANUS KINASE 2 V617F MUTATION, BLOODJAK2
JANUS KINASE 2 V617F MUTATION, NON-BLOODNJAK2
KIT D816V MUTATION BY AS-PCR, BLOODD816V
KIT D816V MUTATION BY AS-PCR, NON-BLOODND816V
KIT SEQUENCING (EXONS 8 AND 17), BLOODCKITMU
KIT SEQUENCING (EXONS 8 AND 17), NON-BLOODNCKIT
KRAS / NRAS MUTATION ANALYSISRAS
MATERNAL CELL CONTAMINATION, FETAL SAMPLEFMCC
MATERNAL CELL CONTAMINATION, MATERNAL SAMPLEMCC
MGMT PROMOTER METHYLATION, BLOODMGMTB
MGMT PROMOTER METHYLATION, NON-BLOODMGMT
MICROSATELLITE INSTABILITYTMSI
MYD88 MUTATION ANALYSIS, BLOODMYD88
MYD88 MUTATION ANALYSIS, NON BLOODNMYD88
PENDRED SYNDROME, BLOODPDS
PENDRED SYNDROME, NON-BLOODNPDS
PML/RARA, QUANTITATIVE, BLOODT1517
PML/RARA, QUANTITATIVE, NON-BLOODBM1517
PRADER-WILLI SYNDROMEPWS
PROTHROMBIN-20210A MUTATION, BLOODP20210
SF3B1 BY SEQUENCING, BLOODSF3B1
SF3B1 BY SEQUENCING, NON-BLOODNSF3B1
STANFORD SOLID TUMOR ACTIONABLE MUTATION PANELSTAMP
T-CELL CLONALITY BY PCR REFLEX TO TCR-BETA (TCRB) REARRANGEMENTS, BLOODTCLON
T-CELL CLONALITY BY PCR REFLEX TO TCR-BETA (TCRB) REARRANGEMENTS, NON-BLOODBMTCLO
VH HYPERMUTATION, BLOODVHHA
VH HYPERMUTATION, NON-BLOODNVHHA

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Special Coagulation View Department Homepage

TESTS:
Select a test to view Test Description & Clinical Indications
TEST CODES:
Select a Test Code to view Test Specimen Collection Instructions
ACTIVATED PROTEIN C RESISTANCE APC
ADAMTS-13 PROFILE ADAMTS
ANTI-PHOSPHOLIPID ANTIBODY PANEL APHSA2
ANTI-THROMBIN III PLASMA AT3
BETA-2 GLYCOPROTEIN 1 B2GP1
CARDIOLIPIN ANTIBODY, IGG AND IGM, SERUM ACA
D-DIMER (ELISA) DDIML
D-DIMER PLASMA, QUALITATIVE DDIM
DILUTE RUSSELL VIPER VENOM DRVVTP
EUGLOBULIN CLOT LYSIS ECL
FACTOR II ASSAY FACT2
FACTOR IX ASSAY FACT9
FACTOR V ASSAY FACT5
FACTOR VII ASSAY FACT7
FACTOR VIII ASSAY FACT8
FACTOR VIII INHIBITOR, HUMAN F8INH
FACTOR X ASSAY FACT10
FACTOR XI ASSAY FACT11
FACTOR XII ASSAY FACT12
FACTOR XIII SCREEN FACT13
FIBRIN DEGRADATION PRODUCTS FDP
FREE PROTEIN S ACTIVITY, PLASMA PROTSF
HEPARIN INDUCED THROMBOCYTOPENIA PANEL HITPNL
HEPARIN PLATELET FACTOR 4 ANTIBODY HITAB
HEPARIN X A (FONDAPARINUX), PLASMA ARIX
HIT FUNCTIONAL BY IMPEDANCE AGGREGOMETRY HITIA
LMWH ACTIVITY BY ANTI-Xa ACTIVITY ANTIXA
LUPUS ANTICOAGULANT - PTTLA LUPUS
PHOSPHATIDYLSERINE/PROTHROMBIN ANTIBODIES LABAPSPT
PLASMINOGEN ACTIVITY PLASMN
PLATELET AGGREGATION PLTAGG
PLATELET FUNCTION SCREEN PLTFUN
PLATELET INHIBITION BY THROMBOELASTOGRAPHY PLATELET MAPPING PLTMAP
PROTEIN C ANTIGEN, TOTAL TOTALC
PROTEIN C, ACTIVITY, PLASMA PROTC
PROTEIN S ANTIGEN, TOTAL TOTALS
PROTEIN S, ACTIVITY, PLASMA PROTS
PT INHIBITOR SCREEN PTINH
PTT INHIBITOR SCREEN PTTINH
REPTILASE TIME REPT
RISTOCETIN-INDUCED PLATELET AGGREGATION RIPA
THROMBIN TIME TT
UNFRACTIONATED HEPARIN ACTIVITY BY ANTI-Xa ACTIVITY HEPAR
VON WILLEBRAND DISEASE SCREEN VWSCN
VON WILLEBRAND FACTOR ACTIVITY VWACT
VON WILLEBRAND FACTOR ANTIGEN PLASMA VWAG

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Flow Cytometry View Department Homepage

TESTS:
Select a test to view Test Description & Clinical Indications
TEST CODES:
Select a Test Code to view Test Specimen Collection Instructions
CD34 PANEL, BLOOD CD34
CD34 PANEL, BONE MARROW BMCD34
CD34 PANEL, FLUID FCD34
CD4-CD8 PANEL, BLOOD C4C8
EMA (EOSIN-5-MALEIMIDE) BY FLOW CYTOMETRY EMA
IMMUNOPHENOTYPING BY FLOW CYTOMETRY FCPATH
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA SCREEN (PNH) SCREEN PATH13/FCPATH PATH13/FCPATH
SÉZARY/T-CELL PANEL PATH18
T SUBSETS AND B LYMPHS, FLUID FTBLYM
T SUBSETS AND B LYMPHS, WHOLE BLOOD TBLYM

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Malignant Hematology Testing Program View Here

 
 


 
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