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Results: 1 to 20 of 70

Tests names and labsConditionsGenes, analytes, and microbesMethods

SmartMeds+ Pharmacogenomic Testing By Innovative GX Health

Innovative Genomics InnovativeGx Health
United States
167
  • T Targeted variant analysis

Psych HealthPGx Panel

RPRD Diagnostics, LLC
United States
4013
  • D Deletion/duplication analysis
  • T Targeted variant analysis

Whole Pharmacogenomics Scan

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

RightMed Mental Health test

OneOme, LLC
United States
615
  • D Deletion/duplication analysis
  • T Targeted variant analysis

Genomind Pharmacogenetic Report

Genomind, Inc. Genomind, Inc
United States
1427
  • T Targeted variant analysis

PGx - Comprehensive Panel

Genesys Diagnostics Genesys Diagnostics, Inc.
United States
120
  • T Targeted variant analysis

PGx - Mental Health Panel

Genesys Diagnostics Genesys Diagnostics, Inc.
United States
110
  • T Targeted variant analysis

DRD2 Gene Myoclonic dystonia, DRD2 related NGS Genetic DNA Test

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

DRD2 Gene DYT11, DRD2 related NGS Genetic DNA Test

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

Gravity Pharmacogenetics Comprehensive Profile

Gravity Diagnostics
United States
8617
  • T Targeted variant analysis

Psychotropic Pharmacogenomics Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
122
  • T Targeted variant analysis

Pharmacogenomics Profile + HLA

AccessDx Lab LLC
United States
7142
  • D Deletion/duplication analysis
  • T Targeted variant analysis

PGx-NP (Neuro-Psychiatry)

SPMED CO., LTD Step forward Personalized Medicine
South Korea
5126
  • T Targeted variant analysis

iDNA PGx-CNS

iDNA Genomics
Greece
3012
  • T Targeted variant analysis

Pharmacogenetics Panel: Psychotropics, with GeneDose Access

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
814
  • E Sequence analysis of select exons

Movement diseases (WES based NGS panel of 931 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
10930
  • C Sequence analysis of the entire coding region

Dystonia (WES based NGS panel of 117 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
1117
  • C Sequence analysis of the entire coding region

Myoclonic dystonia (DYT11, deletion/duplication analysis on DRD2 gene)

CGC Genetics Unilabs
Portugal
11
  • D Deletion/duplication analysis

Myoclonic dystonia (DYT11, sequence analysis of DRD2 gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

HEREDITARY ATAXIAS EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
11202
  • E Sequence analysis of select exons

Results: 1 to 20 of 70

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.