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Results: 1 to 20 of 25 (representing 16 labs)

Tests names and labsConditionsGenes and analytesMethods

Cardiomyopathy, familial hypertrophic, 16

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

Pan Cardiomyopathy Sequencing Panel

PreventionGenetics
United States
8882
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hypertrophic Cardiomyopathy Sequencing Panel

PreventionGenetics
United States
4438
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Cardiology Sequencing Panel

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

FAMILIAL DILATED CARDIOMYOPATHY/HYPERTROPHIC/NONCOMPACTION: NGS PANEL

Laboratorio de Genetica Clinica SL
Spain
5353
  • C Sequence analysis of the entire coding region

Comprehensive Cardiac Panel

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

MYOZ2 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
11
  • 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

Hypertrophic Cardiomyopathy

Asper Biogene Asper Biogene LLC
Estonia
2528
  • 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

Comprehensive Cardiovascular: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
42106
  • C Sequence analysis of the entire coding region

Cardiomyopathy, familial hypertrophic 16 (sequence analysis of MYOZ2 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Cardiomyopathy, hypertrophic Panel

CeGaT GmbH
Germany
2230
  • 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

MYOZ2

Fulgent Genetics
United States
11
  • 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

Cardiomyopathy: Sequencing and Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
229106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 25

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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