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Results: 1 to 20 of 33

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

Atrial fibrillation type 3

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

Familial Atrial Fibrillation Syndrome NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
1015
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Cardiac Arrhythmia NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
5246
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Long QT Syndrome and Jervell and Lange-Nielsen syndrome via the KCNQ1 Gene

PreventionGenetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

nucSEEKĀ® Comprehensive Sequence Analysis Of The Nuclear Mitochondrial Exome

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
560420
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Long QT NGS Panel

DDC Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
3111
  • C Sequence analysis of the entire coding region

Short QT Syndrome NGS Panel

DDC Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
146
  • C Sequence analysis of the entire coding region

Atrial Fibrillation and Short QT Syndrome Panel

CeGaT GmbH
Germany
1117
  • C Sequence analysis of the entire coding region

KCNQ1 Gene Sequencing

DDC Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
51
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cardiomyopathy and Arrhythmia Panel, Sequencing (85 Genes) and Deletion/Duplication (83 Genes)

ARUP Laboratories, Molecular Genetics University of Utah ARUP Lab
United States
14785
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy and Arrhythmia Deletion/Duplication, 83 Genes

ARUP Laboratories, Molecular Genetics University of Utah ARUP Lab
United States
14283
  • D Deletion/duplication analysis

Cardiomyopathy and Arrhythmia Panel, Sequencing, 85 Genes

ARUP Laboratories, Molecular Genetics University of Utah ARUP Lab
United States
14785
  • C Sequence analysis of the entire coding region

KCNQ1

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Jervell and Lange-Nielsen Syndrome NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
72
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hearing Loss: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
15992
  • C Sequence analysis of the entire coding region

Sudden Cardiac Arrest (SCA): Sequencing and Deletion/Duplication Panel

Emory Genetics Laboratory Emory University
United States
3010
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Long and Short QT Syndrome: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
3212
  • C Sequence analysis of the entire coding region

Arrhythmias: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
6029
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 33

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.