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Results: 1 to 13 of 13 (representing 10 labs)

Tests names and labsConditionsGenes and analytesMethods

Cardiomyopathy, familial hypertrophic, 19

Centogene AG - the Rare Disease Company
Germany
11
  • 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

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

CALR3 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

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

Cardiomyopathy, hypertrophic Panel

CeGaT GmbH
Germany
2230
  • C Sequence analysis of the entire coding region

CALR3

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Sudden Death Syndrome NGS Panel

Fulgent Genetics
United States
18568
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy, familial hypertrophic (sequence analysis of CALR3 gene)

CGC Genetics
Portugal
31
  • C Sequence analysis of the entire coding region

Cardiomyopathy panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
13461
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Pan-Cardio NGS Panel

Fulgent Genetics
United States
238101
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 13 of 13

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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