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Results: 21 to 37 of 37

Tests names and labsConditionsGenes, analytes, and microbesMethods

PGx-NP (Neuro-Psychiatry)

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

PGx-Premium (Preemptive PGx test)

SPMED CO., LTD Step forward Personalized Medicine
South Korea
6627
  • T Targeted variant analysis

PGx-ADHD

SPMED CO., LTD Step forward Personalized Medicine
South Korea
34
  • T Targeted variant analysis

ABCB1-Related Disorders via the ABCB1 Gene

PreventionGenetics, part of Exact Sciences
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Colchicine resistance, 120080 (ABCB1 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

Inflammatory bowel disease 13, 612244; IBD13 (ABCB1 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

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

Dyslipidemia and early atherosclerosis panel. 84-gene NGS panel.

Genologica Medica
Spain
13384
  • C Sequence analysis of the entire coding region

MDR1 Mutation

Duzen Laboratories Duzen BBAGUAS
Turkey
21
  • T Targeted variant analysis

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Pain Syndromes (NGS Panel and Copy Number Analysis)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
727
  • C Sequence analysis of the entire coding region

Inflammatory bowel disease: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1010
  • C Sequence analysis of the entire coding region

Epilepsy Drug Metabolism Gene mutation panel

Molecular Diagnostics Children's Hospital of Wisconsin
United States
64
  • T Targeted variant analysis

Pharmacogenetic panel

MVZ diagnosticum Frankfurt MVZ diagnosticum GmbH
Germany
4629
  • T Targeted variant analysis

MDR1

MVZ Dr. Eberhard & Partner Dortmund
Germany
21
  • E Sequence analysis of select exons

ABCB1 Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 37 of 37

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.