Clinical and research tests for C1832932 - Genetic Testing Registry (GTR) - NCBI

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Results: 1 to 17 of 17

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel Otogenetics United States	123	129	E Sequence analysis of select exons
CentoHear Panel Centogene US, LLC - The Rare Disease Company United States	203	194	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CentoHear Panel Centogene AG - the Rare Disease Company Germany	203	194	D Deletion/duplication analysis C Sequence analysis of the entire coding region
OtoSCOPE v9 Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States	288	218	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Deafness, autosomal dominant 5, 600994, Autosomal dominant (Autosomal dominant non-syndromic sensorineural deafness type DFNA) (DFNA5 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Genetic Diagnosis and Research Centre Turkey	1	1	C Sequence analysis of the entire coding region
Hereditary Hearing Loss and Deafness Panel PreventionGenetics United States	356	209	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Deafness, autosomal dominant 5 (sequence analysis of DFNA5 gene) Unilabs Genetics CGC Genetics Portugal	1	1	C Sequence analysis of the entire coding region
Hearing Loss, Comprehensive Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	142	84	C Sequence analysis of the entire coding region
Deafness, autosomal dominant: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	40	39	C Sequence analysis of the entire coding region
Hearing Loss Advanced Sequencing and CNV Evaluation Athena Diagnostics Inc United States	249	184	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Autosomal Dominant Hereditary Hearing Loss/Deafness , Panel Massive Sequencing (NGS) 31 Genes Reference Laboratory Genetics Spain	31	31	C Sequence analysis of the entire coding region
Hearing Loss NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	108	91	C Sequence analysis of the entire coding region
DEAFNESS A.D. and A.R. GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Spain	65	57	C Sequence analysis of the entire coding region
DEAFNESS A.D. GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Spain	24	26	C Sequence analysis of the entire coding region
Sensorineural Hearing Loss Asper Biogene Asper Biogene LLC Estonia	83	79	E Sequence analysis of select exons C Sequence analysis of the entire coding region
Hereditary Hearing Loss-Common and Non-Syndromic Hearing Loss Panel Genome Diagnostics Laboratory The Hospital for Sick Children Canada	64	57	D Deletion/duplication analysis C Sequence analysis of the entire coding region
DFNA 5 Nonsyndromic Hearing Loss and Deafness Bioscientia GmbH Center for Human Genetics Germany	1	1	C Sequence analysis of the entire coding region

Results: 1 to 17 of 17

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