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Results: 1 to 20 of 269

Tests names and labsConditionsGenes, analytes, and microbesMethods

TYR - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

LQTS panel

Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS
Italy
113
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiology Sequencing- Congenital heart Disease Panel (24 Genes)

Genesys Diagnostics Genesys Diagnostics, Inc.
United States
2424
  • X Mutation scanning of select exons

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

SCN5A Gene Atrial fibrillation type 10 NGS Genetic DNA Test

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

SCN5A Gene Heart block, progressive, familial, type 1A NGS Genetic DNA Test

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

SCN5A Gene Long QT syndrome type 3 NGS Genetic DNA Test

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

SCN5A Gene Sick sinus syndrome type 1 NGS Genetic DNA Test

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

SCN5A Gene Sudden infant death syndrome, susceptibility to NGS Genetic DNA Test

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

SCN5A Gene Ventricular fibrillation, paroxysmal familial type 1 NGS Genetic DNA Test

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

SCN5A Gene Brugada syndrome type 1 NGS Genetic DNA Test

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

SCN5A Gene Cardiomyopathy, dilated type 1E 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

Comprehensive Cardiomyopathy Panel

Mayo Clinic Laboratories Mayo Clinic
United States
6883
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Long QT Syndrome Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
1210
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Dilated Cardiomyopathy/LVNC Panel

Mayo Clinic Laboratories Mayo Clinic
United States
5263
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Brugada Syndrome, SCN5A Full Gene

Mayo Clinic Laboratories Mayo Clinic
United States
121
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NewbornGeneID

GeneID Lab - Advanced Molecular Diagnostics
United States
7361
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 269

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.