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Results: 1 to 17 of 17

Tests names and labsConditionsGenes, analytes, and microbesMethods

NEURODEVELOPMENTpgx

Eugenomic S.L.
Spain
116
  • T Targeted variant analysis

CARDIOpgx

Eugenomic S.L.
Spain
116
  • T Targeted variant analysis

GLOBALpgx

Eugenomic S.L.
Spain
121
  • T Targeted variant analysis

CYP2C8 Genotyping

IU Genetic Testing Laboratories Indiana University School of Medicine
United States
11
  • T Targeted variant analysis

Rhabdomyolysis and metabolic muscle diseases (WES based NGS panel of 55 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
155
  • C Sequence analysis of the entire coding region

MUSCULAR DISORDERS- EMCG GLOBAL EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1416
  • E Sequence analysis of select exons

Cytochrome P450 Genotyping Panel, with GeneDose Access

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
97
  • T Targeted variant analysis

Pharmacogenetics Genetic Panel (2 Day STAT TAT)

Machaon Diagnostics
United States
38
  • D Deletion/duplication analysis
  • T Targeted variant analysis

Warfarin Sensitivity (CYP2C9, CYP2C cluster, CYP4F2, VKORC1) Genotyping

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
14
  • E Sequence analysis of select exons

Cytochrome P450 Genotyping Panel

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
97
  • T Targeted variant analysis

CYP2C8, CYP2C9, and CYP2C cluster

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
11
  • T Targeted variant analysis

Pioglitazone response

Xcode Life
India
11
  • T Targeted variant analysis

Rosiglitazone response

Xcode Life
India
11
  • T Targeted variant analysis

Rosiglitazone response

Xcode Life
India
11
  • T Targeted variant analysis

Pioglitazone response

Xcode Life
India
11
  • T Targeted variant analysis

CYP2C8 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 17 of 17

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.