Clinical and research tests for C3809007 - Genetic Testing Registry (GTR) - NCBI

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Results: 41 to 60 of 73

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Hereditary leukemia panel. NGS panel of 39 genes. Genologica Medica Spain	89	39	C Sequence analysis of the entire coding region
Noonan syndrome panel. NGS panel of 22 genes. Genologica Medica Spain	48	22	C Sequence analysis of the entire coding region
Cardiofaciocutaneous syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	4	4	C Sequence analysis of the entire coding region
MAP2K2 Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	1	1	D Deletion/duplication analysis
Comprehensive Short Stature Genetic Panel MNG Laboratories (Medical Neurogenetics, LLC.) United States	82	60	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
Cardiomyopathy Panel, Comprehensive CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	170	71	C Sequence analysis of the entire coding region
Cardiomyopathy Panel, Hypertrophic CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	85	35	C Sequence analysis of the entire coding region
Cardiomyopathy Panel, Dilated CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	134	48	C Sequence analysis of the entire coding region
Noonan Spectrum Disorders Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	36	13	C Sequence analysis of the entire coding region
MAP2K2 Institute for Human Genetics University Medical Center Freiburg Germany	1	1	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
Noonan and RASopathies NGS Panel Fulgent Genetics United States	235	26	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Congenital Heart Defect NGS Panel Fulgent Genetics United States	377	114	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CARDIOFACIOCUTANEOUS SYNDROME Laboratorio de Genetica Clinica SL Spain	4	4	C Sequence analysis of the entire coding region
Comprehensive Cardiac NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	174	108	C Sequence analysis of the entire coding region
Noonan Spectrum Disorders Panel Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States	24	21	D Deletion/duplication analysis C Sequence analysis of the entire coding region
PreSeek™ Non-invasive Prenatal Gene Sequencing Screen Baylor Genetics United States	48	30	C Sequence analysis of the entire coding region
Epilepsy Comprehensive NGS Panel Fulgent Genetics United States	729	398	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Congenital Heart Defects and Heterotaxy Panel Labcorp Genetics (formerly Invitae) LabCorp United States	128	82	D Deletion/duplication analysis C Sequence analysis of the entire coding region

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Results: 41 to 60 of 73

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.