Clinical and research tests for 608616 - Genetic Testing Registry (GTR) - NCBI

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Results: 1 to 19 of 19

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Mucopolysaccharidosis type IIID (deletion/duplication analysis of GNS gene) CGC Genetics Unilabs Portugal	1	1	D Deletion/duplication analysis
Cardiomyopathies General Panel Health in Code Spain	1	173	C Sequence analysis of the entire coding region
Hypertrophic cardiomyopathy extended panel Health in Code Spain	1	104	C Sequence analysis of the entire coding region
Arrhythmia General Panel Health in Code Spain	1	218	C Sequence analysis of the entire coding region
Cardiovascular Diseases_General Panel Health in Code Spain	1	380	C Sequence analysis of the entire coding region
Dilated Cardiomyopathy panel Clinical Genomics Laboratory Washington University in St. Louis United States	1	68	C Sequence analysis of the entire coding region
Cardiomyopathy panel Clinical Genomics Laboratory Washington University in St. Louis United States	5	96	C Sequence analysis of the entire coding region
Cardiac Diseases Gene panel Clinical Genomics Laboratory Washington University in St. Louis United States	12	150	C Sequence analysis of the entire coding region
Rhabdomyolysis and metabolic muscle diseases (WES based NGS panel of 55 genes, including CNV analysis) CGC Genetics Unilabs Portugal	1	55	C Sequence analysis of the entire coding region
MITOCHONDRIAL DISEASES PANEL (NUCLEAR GENES) Laboratorio de Genetica Clinica SL Spain	1	1372	E Sequence analysis of select exons
HYPERTROPHIC CARDIOMYOPATHY EXOME PANEL Laboratorio de Genetica Clinica SL Spain	1	197	E Sequence analysis of select exons
SUDDEN DEATH/ IDIOPATHIC VENTRICULAR FIBRILLATION EXOME PANEL Laboratorio de Genetica Clinica SL Spain	1	394	E Sequence analysis of select exons
DILATED CARDIOMYOPATHY EXOME PANEL Laboratorio de Genetica Clinica SL Spain	1	141	E Sequence analysis of select exons
Autism/ID Xpanded Panel GeneDx United States	2	2592	D Deletion/duplication analysis C Sequence analysis of the entire coding region
OBSCN Single Gene Fulgent Genetics United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hypertrophic Cardiomyopathy Panel Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University United States	1	36	C Sequence analysis of the entire coding region
Cardiomyopathy Panel Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University United States	13	112	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cardiomyopathy and Arrhythmia Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	125	83	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

Results: 1 to 19 of 19

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.