Clinical and research tests for C1858672 - Genetic Testing Registry (GTR) - NCBI

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Results: 21 to 40 of 72

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Complete epilepsy panel. NGS panel of 283 genes. Genologica Medica Spain	409	283	C Sequence analysis of the entire coding region
Atrial fibrillation panel. NGS panel of 19 genes. Genologica Medica Spain	55	19	C Sequence analysis of the entire coding region
Brugada syndrome panel. 9-gene NGS panel. Genologica Medica Spain	26	9	C Sequence analysis of the entire coding region
Early Infantile Epileptic Encephalopathy NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	114	86	C Sequence analysis of the entire coding region
Epilepsy Panel, Febrile CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	35	17	C Sequence analysis of the entire coding region
Brugada Syndrome Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	25	14	C Sequence analysis of the entire coding region
Arrhythmia & Cardiomyopathy Panel, Comprehensive CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	211	93	C Sequence analysis of the entire coding region
Arrhythmia Panel, Comprehensive CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	71	36	C Sequence analysis of the entire coding region
Epilepsy Panel, STAT CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	44	21	C Sequence analysis of the entire coding region
Epilepsy Panel, Comprehensive CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	132	83	C Sequence analysis of the entire coding region
SCN1B Institute for Human Genetics University Medical Center Freiburg Germany	4	1	C Sequence analysis of the entire coding region
Epilepsy, generalized, with febrile seizures plus: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	11	6	C Sequence analysis of the entire coding region
Childhood Epilepsy NGS Panel Fulgent Genetics United States	354	209	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Neonatal Epilepsy NGS Panel Fulgent Genetics United States	509	275	D Deletion/duplication analysis 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
Dravet Syndrome NGS Panel Fulgent Genetics United States	27	11	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Neuromuscular Channelopathies , Panel Massive Sequencing (NGS) 44 Genes Reference Laboratory Genetics Spain	60	44	C Sequence analysis of the entire coding region
Severe Myoclonic Epilepsy (Dravet's Syndrome), Panel Massive Sequencing (NGS) 11 Genes Reference Laboratory Genetics Spain	11	11	C Sequence analysis of the entire coding region

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Results: 21 to 40 of 72

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.