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Results: 1 to 20 of 30 (representing 14 labs)

Tests names and labsConditionsGenes and analytesMethods

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

Dilated Cardiomyopathy Sequencing Panel

PreventionGenetics
United States
3332
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

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

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

Invitae Cardiomyopathy and Skeletal Muscle Disease Panel

Invitae
United States
190150
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CARDIOMYOPATHY, DILATED (DCM

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
3132
  • C Sequence analysis of the entire coding region

Invitae Dilated Cardiomyopathy Panel

Invitae
United States
4162
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Cardiomyopathy Comprehensive Panel

Invitae
United States
8179
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel

Invitae
United States
127112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Arrhythmia Comprehensive Panel

Invitae
United States
7362
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial isolated restrictive cardiomyopathy

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

TNNI3

Institute for Human Genetics University Clinic Freiburg
Germany
41
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy NGS Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
4823
  • C Sequence analysis of the entire coding region

Restrictive Cardiomyopathy NGS Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
3210
  • C Sequence analysis of the entire coding region

Cardiomyopathy, dilated, 1FF

MVZ Dortmund Dr. Eberhard and Partner
Germany
41
  • C Sequence analysis of the entire coding region

Cardiomyopathy, dilated, 1FF

MVZ Dortmund Dr. Eberhard and Partner
Germany
41
  • C Sequence analysis of the entire coding region

TNNI3

Fulgent Genetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy NGS Panel

Fulgent Genetics
United States
15063
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 30

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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