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Results: 1 to 20 of 129 (representing 44 labs)

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
7861205
  • C Sequence analysis of the entire coding region

Amyloidosis

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

Pan Cardiomyopathy Panel (62 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
10361
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HCM Panel (20 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
4220
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DCM/Arrhythmogenic Cardiomyopathy Panel (53 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
9853
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial Transthretin Amyloidosis

Molecular Diagnostics Laboratory University Health Network
Canada
11
  • C Sequence analysis of the entire coding region

Familial Transthyretin Amyloidosis

Molecular Genetics Laboratory London Health Sciences Centre
Canada
11
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • E Sequence analysis of select exons

Comprehensive Neuropathy Sequencing Panel

PreventionGenetics
United States
8271
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cardiomyopathy Exome Panel

Northwest Clinical Genomics Laboratory University of Washington
United States
3275
  • C Sequence analysis of the entire coding region

Cardiomyopathies General Panel

Health in Code S.L.
Spain
1173
  • C Sequence analysis of the entire coding region

Resctrictive cardiomyopathy

Health in Code S.L.
Spain
120
  • C Sequence analysis of the entire coding region

Hypertrophic cardiomyopathy extended panel

Health in Code S.L.
Spain
1104
  • C Sequence analysis of the entire coding region

Arrhythmia General Panel

Health in Code S.L.
Spain
1218
  • C Sequence analysis of the entire coding region

Atrial fibrillation Panel

Health in Code S.L.
Spain
143
  • C Sequence analysis of the entire coding region

Cardiac conduction disease Panel

Health in Code S.L.
Spain
134
  • C Sequence analysis of the entire coding region

Hypertrophic cardiomyopathy panel

Health in Code S.L.
Spain
117
  • C Sequence analysis of the entire coding region

Cardiovascular Diseases_General Panel

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

Ventricular arrhythmia and sudden death without structural heart disease

Health in Code S.L.
Spain
177
  • C Sequence analysis of the entire coding region

Familial transthyretin amyloidosis (TTR)

Health in Code S.L.
Spain
11
  • C Sequence analysis of the entire coding region

Charcot Marie Tooth Panel

Molecular Genetics Laboratory London Health Sciences Centre
Canada
4634
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 1 to 20 of 129

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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