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Results: 21 to 40 of 127

Tests names and labsConditionsGenes, analytes, and microbesMethods

Invitae 78 Gene Actionable Disorders Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
22075
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Carrier Screen

Labcorp Genetics (formerly Invitae) LabCorp
United States
886547
  • D Deletion/duplication analysis
  • 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

CPVTNext®

Ambry Genetics
United States
64
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CardioNext®

Ambry Genetics
United States
18992
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

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

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

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 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 Deletion/ Duplication panel

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

Sudden Cardiac Arrest Panel

PreventionGenetics, part of Exact Sciences
United States
6349
  • 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
224202
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
327300
  • C Sequence analysis of the entire coding region

Cardiac Arrhythmia Exome Panel

Northwest Clinical Genomics Laboratory University of Washington
United States
3951
  • C Sequence analysis of the entire coding region

Cardiomyopathy Exome Panel

Northwest Clinical Genomics Laboratory University of Washington
United States
3275
  • C Sequence analysis of the entire coding region

Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
239100
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Arrhythmia Comprehensive Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
11541
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 127

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.