Clinical and research tests for C2348199 - Genetic Testing Registry (GTR) - NCBI

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Results: 21 to 40 of 46

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Rest of Combined Cardiac after Arrhythmia Panel GeneDx United States	5	80	D Deletion/duplication analysis C Sequence analysis of the entire coding region
SCA Arrhythmia Panel GeneDx United States	5	14	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Rest of Arrhythmia after Brugada Syndrome Panel GeneDx United States	5	41	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Arrhythmia Sequencing and Del/Dup Panel GeneDx United States	5	58	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Combined Cardiac Sequencing and Del/Dup Panel GeneDx United States	10	138	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Custom Cardiology Sequencing and Del/Dup Panel GeneDx United States	30	270	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Phosphorus Short QT Syndrome Panel Phosphorus Diagnostics LLC United States	1	6	D Deletion/duplication analysis C Sequence analysis of the entire coding region
KCNH2 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	2	1	C Sequence analysis of the entire coding region T Targeted variant analysis
KCNQ1 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	2	1	C Sequence analysis of the entire coding region T Targeted variant analysis
CACNA1C Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	3	1	C Sequence analysis of the entire coding region T Targeted variant analysis
CACNA2D1 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	2	1	C Sequence analysis of the entire coding region T Targeted variant analysis
CACNB2 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	2	1	C Sequence analysis of the entire coding region T Targeted variant analysis
KCNJ2 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	4	1	C Sequence analysis of the entire coding region T Targeted variant analysis
Short QT Syndrome Panel by NGS Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	1	6	C Sequence analysis of the entire coding region T Targeted variant analysis
Short QT Syndrome (SQTS) Panel Blueprint Genetics Finland	1	5	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Cardiology Panel Blueprint Genetics Finland	12	185	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Arrhythmia Panel Blueprint Genetics Finland	7	55	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Long QT Syndrome and Short QT Syndrome Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University United States	6	13	C Sequence analysis of the entire coding region
Comprehensive Arrhythmias Panel Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University United States	7	23	C Sequence analysis of the entire coding region
Short QT Syndrome Panel Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	8	6	C Sequence analysis of the entire coding region

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Results: 21 to 40 of 46

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.