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Results: 1 to 20 of 37 (representing 16 labs)

Tests names and labsConditionsGenes and analytesMethods

Cardiomyopathy, familial restrictive type 1

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

Comprehensive Cardiology Sequencing Panel

PreventionGenetics
United States
190164
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Cardiac Arrhythmia Sequencing Panel

PreventionGenetics
United States
6855
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

TNNI3. Complete sequencing

Instituto de Medicina Genomica
Spain
71
  • C Sequence analysis of the entire coding region

MYL3. Complete sequencing

Instituto de Medicina Genomica
Spain
71
  • C Sequence analysis of the entire coding region

ACTC1. Complete sequencing

Instituto de Medicina Genomica
Spain
71
  • C Sequence analysis of the entire coding region

MYH7, MYBPC3, TNNT2, TNNI3, TPM1, MYL3, ACTC1. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
77
  • C Sequence analysis of the entire coding region

TNNT2. Complete sequencing

Instituto de Medicina Genomica
Spain
61
  • C Sequence analysis of the entire coding region

LMNA. Complete sequencing

Instituto de Medicina Genomica
Spain
61
  • C Sequence analysis of the entire coding region

MYL2. Complete sequencing

Instituto de Medicina Genomica
Spain
71
  • C Sequence analysis of the entire coding region

MYH7. Complete sequencing

Instituto de Medicina Genomica
Spain
61
  • C Sequence analysis of the entire coding region

ACTC1, MYBPC3, MYH6, MYH7, MYL2, MYL3, TCAP, TNNC1, TNNI3, TNNT2, TPM1. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
1111
  • C Sequence analysis of the entire coding region

LMNA, MYBPC3, MYH7, SCN5A, TNNI3, TNNT2. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
66
  • C Sequence analysis of the entire coding region

TNNI3. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy and Related Disorders via the TNNI3 Gene

PreventionGenetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Cardiac Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
174107
  • C Sequence analysis of the entire coding region

TNNI3 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
41
  • C Sequence analysis of the entire coding region

Results: 1 to 20 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.

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