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Results: 1 to 20 of 125

Tests names and labsConditionsGenes, analytes, and microbesMethods

Precision HealthPGx Panel (25 Genes)

RPRD Diagnostics, LLC
United States
9723
  • D Deletion/duplication analysis
  • T Targeted variant analysis

Admera Health PGxOne™ Plus

Admera Health
United States
9916
  • T Targeted variant analysis

Whole Pharmacogenomics Scan

RPRD Diagnostics, LLC
United States
10769
  • D Deletion/duplication analysis
  • T Targeted variant analysis

Tempus xT

Tempus AI - RTP
United States
2647
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

DPYD Genotyping

Sanford Medical Genetics Laboratory Sanfordhealth
United States
41
  • T Targeted variant analysis

DPYD Gene Dihydropyrimidine dehydrogenase deficiency NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Genetic study of pharmacogenetics

HeartGenetics, Genetics and Biotechnology, SA
Portugal
126
  • T Targeted variant analysis

Dihydropyrimidine Dehydrogenase Genotype

Mayo Clinic Laboratories Mayo Clinic
United States
41
  • T Targeted variant analysis

DPYD Full Gene Sequencing

Mayo Clinic Laboratories Mayo Clinic
United States
41
  • C Sequence analysis of the entire coding region

Pharmacogenetic Panel

Sanford Medical Genetics Laboratory Sanfordhealth
United States
514
  • T Targeted variant analysis

Tempus xT

Tempus AI - CHI
United States
2647
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

Tempus xF

Tempus AI - RTP
United States
1105
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

DPYD genotyping

Molecular Genetics Laboratory North York General Hospital
Canada
11
  • T Targeted variant analysis

Pharmacogenomics Profile + HLA

AccessDx Lab LLC
United States
7138
  • D Deletion/duplication analysis
  • T Targeted variant analysis

CentoMetabolic MOx

Centogene AG - the Rare Disease Company
Germany
195205
  • A Analyte
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoScreen

Centogene AG - the Rare Disease Company
Germany
316314
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

DPYD - NGS including CNV analysis

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

CentoNeuro Panel

Centogene AG - the Rare Disease Company
Germany
18861858
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Epilepsy Panel

Centogene AG - the Rare Disease Company
Germany
734744
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Intellectual Disability Panel

Centogene AG - the Rare Disease Company
Germany
777770
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 1 to 20 of 125

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.