Clinical and research tests for SCN4B - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
LQTS panel Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS Italy	1	13	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cardiology Sequencing- Arrhythmia Comprehensive Panel (134 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States	88	134	X Mutation scanning of select exons
Cardiology Sequencing- Full Panel (174 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States	122	174	X Mutation scanning of select exons
SCN4B Gene Long QT syndrome type 10 NGS Genetic DNA Test DNA Labs India India	1	1	S Mutation scanning of the entire coding region
GenepoweRx_Cardiac Care GenepoweRx Uppaluri K&H Personalized Medicine Clinic India	63	102	D Deletion/duplication analysis H Detection of homozygosity S Mutation scanning of the entire coding region T Targeted variant analysis
SCN4B - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CentoCardio Panel Centogene AG - the Rare Disease Company Germany	289	275	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Long QT Syndrome Panel PreventionGenetics, part of Exact Sciences United States	22	19	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Cardiac channelopathy Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	1	41	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Cardiac channelopathy NGS panel HNL Genomics Connective Tissue Gene Tests United States	1	41	C Sequence analysis of the entire coding region T Targeted variant analysis
Atrial fibrillation Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	1	21	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Long QT syndrome NGS panel HNL Genomics Connective Tissue Gene Tests United States	26	19	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	1	41	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Long QT syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	26	19	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Long QT syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States	26	19	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Atrial fibrillation NGS panel HNL Genomics Connective Tissue Gene Tests United States	1	21	C Sequence analysis of the entire coding region T Targeted variant analysis
Atrial fibrillation Deletion/ Duplication panel HNL Genomics Connective Tissue Gene Tests United States	1	21	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Atrial fibrillation, familial, 17, 611819, Autosomal dominant (Familial long QT syndrome) (SCN4B gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Long QT syndrome-10, 611819, Autosomal dominant; LQT10 (Familial long QT syndrome) (SCN4B gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Cardiac channelopathies panel Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS Italy	9	33	S Mutation scanning of the entire coding region

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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.