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Results: 1 to 20 of 47

Tests names and labsConditionsGenes, analytes, and microbesMethods

Pan Cardiomyopathy Panel (62 Genes)

Laboratory for Molecular Medicine Mass General Brigham Personalized Medicine
United States
10161
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ABCC9 - NGS including CNV analysis

Centogene US, LLC - The Rare Disease Company
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ABCC9 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Overgrowth Syndromes Panel

Invitae
United States
11356
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy, dilated, 1O, 608569; CMD1O (Familial isolated dilated cardiomyopathy) (ABCC9 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

DCMNext®

Ambry Genetics
United States
10137
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CustomNext-Cardio®

Ambry Genetics
United States
237167
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CMNext®

Ambry Genetics
United States
13956
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CardioNext®

Ambry Genetics
United States
19092
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Dilated Cardiomyopathy and Left Ventricular Noncompaction Panel

Invitae
United States
13554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Cardiomyopathy Comprehensive Panel

Invitae
United States
19982
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel

Invitae
United States
240100
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Arrhythmia Comprehensive Panel

Invitae
United States
11541
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cantu Syndrome via the ABCC9 Gene

PreventionGenetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Dilatative Cardiomyopathy Panel (DCM Panel)

Labor Dr. Wisplinghoff
Germany
4343
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Arrhythmia panel. NGS panel of 55 genes.

Genologica Medica
Spain
12855
  • C Sequence analysis of the entire coding region

Brugada syndrome (WES based NGS panel of 23 genes, including CNV analysis)

Unilabs Genetics CGC Genetics
Portugal
3323
  • C Sequence analysis of the entire coding region

Dilated cardiomyopathy (WES based NGS panel of 81 genes, including CNV analysis)

Unilabs Genetics CGC Genetics
Portugal
17981
  • C Sequence analysis of the entire coding region

Cardiomyopathy (hypertrophic, dilated , arrhythmogenic right ventricular dysplasia and left ventricular noncompaction) and changes in cardiac conduction (WES based NGS panel of 140 genes, including CNV analysis)

Unilabs Genetics CGC Genetics
Portugal
268140
  • C Sequence analysis of the entire coding region

Cardiomyopathy, dilated 1O (sequence analysis of ABCC9 gene)

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

Results: 1 to 20 of 47

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.