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Results: 1 to 20 of 103

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

SCN3B Gene Brugada syndrome type 7 NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning 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

SCN3B - 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

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

Atrial fibrillation Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
121
  • D Deletion/duplication analysis
  • 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

Brugada syndrome and related disorders Deletion/ Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
125
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Brugada syndrome and related disorders Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
125
  • 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
125
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Atrial fibrillation NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
121
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Atrial fibrillation Deletion/ Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
121
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Atrial fibrillation, familial, 16, 613120, Autosomal dominant (Brugada syndrome) (SCN3B 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

Brugada syndrome 7, 613120, Autosomal dominant; BRGDA7 (Brugada syndrome) (SCN3B 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

Cardiac channelopathies panel

Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS
Italy
933
  • S Mutation scanning of the entire coding region

RhythmNext®

Ambry Genetics
United States
9142
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CustomNext-Cardio®

Ambry Genetics
United States
236167
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 103

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.