Clinical and research tests for C0085298 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Cardiovascular Diseases_General Panel Health in Code Spain	1	380	C Sequence analysis of the entire coding region
Catecholaminergic Polymoprhic Ventricular Tachycardia Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS Italy	3	6	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cardiomyopathies Panel Health in Code Spain	1	149	C Sequence analysis of the entire coding region
Inherited Cardiovascular Diseases and Sudden Death Panel Health in Code Spain	1	213	C Sequence analysis of the entire coding region
Comprehensive Cardiomyopathy NGS Panel Fulgent Genetics United States	450	128	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Long QT/Brugada Syndrome NGS Panel Fulgent Genetics United States	69	34	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Arrhythmogenic Right Ventricular Cardiomyopathy NGS Panel Fulgent Genetics United States	118	46	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
CALM3 Single Gene Fulgent Genetics United States	2	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CALM2 Single Gene Fulgent Genetics United States	5	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CTSH Single Gene Fulgent Genetics United States	10	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
P2RY11 Single Gene Fulgent Genetics United States	10	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CEP85L Single Gene Fulgent Genetics United States	6	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
GPD1L Single Gene Fulgent Genetics United States	11	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Catecholaminergic Polymorphic Ventricular Tachycardia NGS Panel Fulgent Genetics United States	19	9	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Clinical Exome Fulgent Genetics United States	5129	4672	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cardiac Arrhythmia NGS Multi-Gene Panel (48 genes), Sequence & CNV analysis Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center, Location AMC Netherlands	7	47	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Sudden Death Syndrome NGS Panel Fulgent Genetics United States	168	68	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Cardiovascular NGS Panel Fulgent Genetics United States	671	250	D Deletion/duplication analysis C Sequence analysis 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.