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Results: 21 to 40 of 52

Tests names and labsConditionsGenes, analytes, and microbesMethods

Invitae Hypertrophic Cardiomyopathy Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
6930
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Glycogen Storage Disease and Disorders of Glucose Metabolism Panel

PreventionGenetics, part of Exact Sciences
United States
3333
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

PRKAG2-Related Disorders via the PRKAG2 Gene

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

Glycogen Storage Disorders Panel, Sequencing

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
4032
  • C Sequence analysis of the entire coding region

Glycogen Storage Diseases Gene Panel

Duzen Laboratories Duzen BBAGUAS
Turkey
2826
  • C Sequence analysis of the entire coding region

PRKAG2 Deletion/duplication analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
31
  • D Deletion/duplication analysis

Arrhythmia & Cardiomyopathy Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
21193
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
17071
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel, Hypertrophic

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
8535
  • C Sequence analysis of the entire coding region

Glycogen Storage Disease Gene Sequencing Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
1919
  • C Sequence analysis of the entire coding region

PRKAG2

Institute for Human Genetics University Medical Center Freiburg
Germany
31
  • C Sequence analysis of the entire coding region

Comprehensive Metabolism NGS Panel

Fulgent Genetics
United States
602355
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Wolff-Parkinson-White Syndrome (PRKAG2 Single Gene Test)

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ACMG Secondary Findings (Medically Actionable Genes, Including Cardio and Cancer) NGS Panel

Fulgent Genetics
United States
17759
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiomyopathy NGS Panel

Fulgent Genetics
United States
450128
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Arrhythmogenic Right Ventricular Cardiomyopathy NGS Panel

Fulgent Genetics
United States
11846
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Glycogen-Storage NGS Panel

Fulgent Genetics
United States
3630
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dilated & Arrhythmogenic Cardiomyopathy NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
9251
  • C Sequence analysis of the entire coding region

Comprehensive Cardiac NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
174108
  • C Sequence analysis of the entire coding region

Metabolic Myopathies Panel

CeGaT GmbH
Germany
2644
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 52

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.