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Results: 1 to 20 of 105

Tests names and labsConditionsGenes and analytesMethods

MyoGene Panel (43 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
9543
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular Dystrophy (LGMD/EDMD) Panel (25 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
6425
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy, dilated type 1A

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
10362
  • 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
9753
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiac Arrhythmia Exome Panel

Northwest Clinical Genomics Laboratory University of Washington
United States
4151
  • 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

TruGenome Predisposition Screen (Whole Genome Sequencing)

Illumina Clinical Services Laboratory Illumina
United States
15391578
  • C Sequence analysis of the entire coding region

ACTC1, DTNA, LDB3, LMNA, MYH7, TAZ, TNNT2. 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

MYH7. Complete sequencing

Instituto de Medicina Genomica
Spain
61
  • 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

Dilated Cardiomyopathy NextGen Sequencing (NGS) panel

PreventionGenetics
United States
3332
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Left Ventricular Noncompaction (LVNC) NextGen Sequencing (NGS) panel

PreventionGenetics
United States
99
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Laminopathies via the LMNA Gene

PreventionGenetics
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Lamin A/C - LMNA Del/Dup Analysis

Molecular Genetics Laboratory Children's Hospital Colorado
United States
111
  • D Deletion/duplication analysis

Lamin A/C - LMNA Sequencing

Molecular Genetics Laboratory Children's Hospital Colorado
United States
111
  • C Sequence analysis of the entire coding region

LMNA Gene Sequencing

GENETIX Centro de Investigación en Genética Humana y Reproductiva
Colombia
111
  • C Sequence analysis of the entire coding region

LMNA

Institute for Human Genetics University Clinic Freiburg
Germany
121
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 105

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.