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Results: 1 to 20 of 21 (representing 10 labs)

Tests names and labsConditionsGenes and analytesMethods

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

OtoGenome Test for Hearing Loss (87 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
11286
  • 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 SYNDROME, JERVELL AND LANGE-NIELSEN SYNDROME (AUTOSOMAL RECESSIVE)

Laboratorio de Genetica Clinica SL
Spain
12
  • C Sequence analysis of the entire coding region

Long QT Syndrome 1 (KCNQ1) Targeted Testing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
21
  • T Targeted variant analysis

Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel

Invitae
United States
10067
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Arrhythmia Comprehensive Panel

Invitae
United States
5939
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Jervell and Lange-Nielsen syndrome (sequence analysis of KCNQ1 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

KCNQ1 Gene Sequencing

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

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

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

KCNQ1

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

Jervell and Lange-Nielsen Syndrome NGS Panel

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

Invitae Long QT Syndrome Panel

Invitae
United States
1813
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
601504
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Short QT NGS Panel

Fulgent Genetics
United States
164
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Sudden Death Syndrome NGS Panel

Fulgent Genetics
United States
18568
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hearing Loss NGS Panel

Fulgent Genetics
United States
202103
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Atrial Fibrillation NGS Panel

Fulgent Genetics
United States
7523
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Long QT syndrome NGS Panel

Fulgent Genetics
United States
4013
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pan-Cardio NGS Panel

Fulgent Genetics
United States
238101
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 21

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.

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