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Results: 1 to 20 of 34

Tests names and labsConditionsGenes and analytesMethods

PharmacoScan

RPRD Diagnostics, LLC
United States
3511
  • T Targeted variant analysis

OneOme RightMed pharmacogenomic test

OneOme
United States
9421
  • D Deletion/duplication analysis
  • T Targeted variant analysis

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

Tempus xO assay

Tempus Labs, Inc.
United States
11714
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Hyperbilirubinemia, Rotor type, digenic

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Next Generation Sequencing for Jaundice Associated Genes Variation Test

National Taiwan University Hospital A1 Center National Taiwan University Hospital
Taiwan
473
  • C Sequence analysis of the entire coding region

152 Integrated Advantage NGS Solid Tumor Panel

Integrated Molecular Diagnostics Pathology, Inc.
United States
6152
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Rxight Pharmacogenetics Program

MD Labs
United States
7920
  • A Analyte

Familial hypercholesterolemia Extended Panel

Health in Code
Spain
123
  • C Sequence analysis of the entire coding region

Dyslipidemias / Early atherosclerosis

Health in Code
Spain
184
  • C Sequence analysis of the entire coding region

Familial hypercholesterolemia Basic Panel

Health in Code
Spain
16
  • C Sequence analysis of the entire coding region

Cardiovascular Diseases_General Panel

Health in Code
Spain
1380
  • C Sequence analysis of the entire coding region

Genetic study of Simvastatin pharmacogenetics

HeartGenetics, Genetics and Biotechnology, SA
Portugal
21
  • T Targeted variant analysis

Rotor Syndrome Sanger Sequencing Panel

PreventionGenetics
United States
12
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Rotor Syndrome via the SLCO1B1 Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

SLCO1B1. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Rotor Syndrome, Sequencing SLCO1B1 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Statin-Induced Myopathy

Asper Biogene Asper Biogene LLC
Estonia
11
  • T Targeted variant analysis

SLCO1B1 genotyping

Alpha Genomix Laboratories
United States
51
  • T Targeted variant analysis

Results: 1 to 20 of 34

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.

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