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Results: 1 to 20 of 30 (representing 15 labs)

Tests names and labsConditionsGenes and analytesMethods

Pan Cardiomyopathy Panel (62 Genes)

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

DCM/Arrhythmogenic Cardiomyopathy Panel (53 Genes)

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

Arrythmogenic Cardiomyopathy Panel

Health in Code S.L.
Spain
5517
  • 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

Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia via the DSG2 Gene

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

Arrhythmogenic Right Ventricular Dysplasia 10 - DSG2 Sequencing

Children's Hospital Colorado Molecular Genetics Laboratory Children's Hospital Colorado
United States
21
  • C Sequence analysis of the entire coding region

Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Panel (ARVD/ARVC Panel)

Labor Dr. Wisplinghoff
Germany
2011
  • 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

DSG2

Institute for Human Genetics University Clinic Freiburg
Germany
21
  • 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

DSG2 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
31
  • C Sequence analysis of the entire coding region

Arrhythmogenic Right Ventricular Cardiomyopathy Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
209
  • C Sequence analysis of the entire coding region

Cardiomyopathy and Arrhythmia Panel, Sequencing (85 Genes) and Deletion/Duplication (83 Genes)

ARUP Laboratories, Molecular Genetics and Genomics
United States
14785
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DSG2

Fulgent Genetics
United States
21
  • 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

Dilated Cardiomyopathy NGS Panel

Fulgent Genetics
United States
8732
  • 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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