U.S. flag

An official website of the United States government

Filters

See more specimen types...
See more states

Other countries

See more countries

Results: 21 to 40 of 65

Tests names and labsConditionsGenes, analytes, and microbesMethods

Pharmacogenetics Panel: Psychotropics

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

OncoAlly™ Solid Tumor Analysis

Variantyx, Inc.
United States
1433
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • R RNA analysis

CoGenesis@Neuro

Codex Genetics Limited
Hong Kong
1490
  • T Targeted variant analysis

RightMed Comprehensive Test with Gene Report

OneOme, LLC
United States
225
  • D Deletion/duplication analysis
  • T Targeted variant analysis

Autism/ID Xpanded Panel

GeneDx
United States
22592
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ataxia Xpanded Panel

GeneDx
United States
1999
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MYOCLONUS DYSTONIA (DYT11)

Laboratorio de Genetica Clinica SL
Spain
25
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Risperidone response

Xcode Life
India
14
  • T Targeted variant analysis

Methadone response

Xcode Life
India
14
  • T Targeted variant analysis

Dystonia

Asper Biogene Asper Biogene LLC
Estonia
3940
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Myoclonic dystonia 11

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Single gene testing DRD2

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

DRD2 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

Dystonia Dyskinesia NGS Panel

Fulgent Genetics
United States
6225
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MVL Vision Panel

Molecular Vision Laboratory
United States
13581028
  • C Sequence analysis of the entire coding region

SLC7A14 - NGS including CNV analysis

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

CentoVision Panel

Centogene AG - the Rare Disease Company
Germany
417413
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Retinitis pigmentosa 68, 615725, Autosomal recessive; RP68 (Retinitis pigmentosa) (SLC7A14 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

qGenEx Intellectual disability

Quantitative Genomic Medicine Laboratories, SL
Spain
31969
  • S Mutation scanning of the entire coding region
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 65

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.