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Results: 1 to 20 of 140

Tests names and labsConditionsGenes, analytes, and microbesMethods

Cardiology Sequencing- Arrhythmia Comprehensive Panel (134 Genes)

Genesys Diagnostics Genesys Diagnostics, Inc.
United States
88134
  • X Mutation scanning of select exons

Cardiology Sequencing- Full Panel (174 Genes)

Genesys Diagnostics Genesys Diagnostics, Inc.
United States
122174
  • X Mutation scanning of select exons

CASQ2 Gene Ventricular tachycardia, catecholaminergic polymorphic type 2 NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Comprehensive Arrhythmia Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
3644
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy and Arrhythmia Panel

Mayo Clinic Laboratories Mayo Clinic
United States
73105
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CPVT Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Catecholaminergic Polymoprhic Ventricular Tachycardia

Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS
Italy
36
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pan Cardiomyopathy Panel (62 Genes)

Laboratory for Molecular Medicine Mass General Brigham Personalized Medicine
United States
10061
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

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

CASQ2 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoCardio Panel

Centogene AG - the Rare Disease Company
Germany
289275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiac channelopathy Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
141
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Catecholaminergic polymorphic ventricular tachycardia Deletion / Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
19
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiac channelopathy NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
141
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cardiac channelopathy Deletion/ Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
141
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Catecholaminergic polymorphic ventricular tachycardia Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
19
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Catecholaminergic polymorphic ventricular tachycardia NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
19
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ventricular tachycardia, catecholaminergic polymorphic, 2, 611938, Autosomal recessive; CPVT2 (Catecholaminergic polymorphic ventricular tachycardia) (CASQ2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Invitae Genetic Health Screen

Invitae
United States
409164
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Cardio Screen

Invitae
United States
20881
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 140

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.