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Results: 1 to 20 of 59 (representing 23 labs)

Tests names and labsConditionsGenes and analytesMethods

Cardiomyopathy, familial hypertrophic type 4

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

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

Hypertrophic Cardiomyopathy Sequencing Panel

PreventionGenetics
United States
1615
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hypertrophic Cardiomyopathy via the MYBPC3 Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Familial hypertrophic cardiomyopathy

Labor Dr. Wisplinghoff
Germany
55
  • C Sequence analysis of the entire coding region

Familial Hypertrophic Cardiomyopathy (MYBPC3) Targeted Testing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
11
  • T Targeted variant analysis

Invitae Cardiomyopathy and Skeletal Muscle Disease Panel

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

CARDIOMYOPATHY HYPERTROPHIC PANEL

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2526
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 59

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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