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Results: 1 to 20 of 23 (representing 13 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

ACTC1, DES, LDB3, MYH6, PSEN1, PSEN2, TCAP, TNNC1, TPM1, VCL. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
1010
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy and Dilated Cardiomyopathy via the VCL Gene

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

VCL 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

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

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

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

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

VCL

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

Left Ventricular Noncompaction NGS Panel

Fulgent Genetics
United States
309
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Hypertrophic Cardiomyopathy Panel

Invitae
United States
2237
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dilated Cardiomyopathy: Sequencing and Deletion/Duplication Panel

Emory Genetics Laboratory Emory University
United States
7438
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy: Sequencing and Deletion/Duplication Panel

Emory Genetics Laboratory Emory University
United States
229106
  • 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

Results: 1 to 20 of 23

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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