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Results: 1 to 18 of 18

Tests names and labsConditionsGenes, analytes, and microbesMethods

GenepoweRx_Cardiac Care

GenepoweRx Uppaluri K&H Personalized Medicine Clinic
India
63102
  • D Deletion/duplication analysis
  • H Detection of homozygosity
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

Non-Immune Hydrops Fetalis Panel

PreventionGenetics, part of Exact Sciences
United States
291148
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Long QT syndrome NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
2619
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Long QT syndrome Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
2619
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Progressive familial heart block type I Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
92
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Progressive familial heart block type I NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
92
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Long QT syndrome NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
2619
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Long QT syndrome Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
2619
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Congenital heart disease NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
1415
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Congenital heart disease Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
1415
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Brugada syndrome and related disorders Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
1826
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Brugada syndrome and related disorders NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
1826
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Pan Cardiomyopathy Panel

PreventionGenetics, part of Exact Sciences
United States
113106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Dilated Cardiomyopathy Panel

PreventionGenetics, part of Exact Sciences
United States
6460
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Cardiology Panel

PreventionGenetics, part of Exact Sciences
United States
223198
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Cardiac Arrhythmia Panel

PreventionGenetics, part of Exact Sciences
United States
7764
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Brugada Syndrome Panel

PreventionGenetics, part of Exact Sciences
United States
917
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Brugada Syndrome 1 via the SCN5A Gene

PreventionGenetics, part of Exact Sciences
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 1 to 18 of 18

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.