Clinical and research tests for C1836027 - Genetic Testing Registry (GTR)

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Results: 41 to 58 of 58

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Hearing Loss Advanced Sequencing and CNV Evaluation Athena Diagnostics United States	249	184	D Deletion/duplication analysis C Sequence analysis of the entire coding region
DEAFNESS, NONSYNDROMIC SENSORINEURAL (AUTOSOMAL RECESSIVE) Laboratorio de Genetica Clinica SL Spain	13	14	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Ashkenazi Jewish Panel Molecular Vision Laboratory United States	12	8	C Sequence analysis of the entire coding region
Hearing Loss NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	198	157	C Sequence analysis of the entire coding region
USHER syndrome panel Molecular Vision Laboratory United States	24	14	C Sequence analysis of the entire coding region
Retinal Dystrophy Panel Molecular Vision Laboratory United States	372	283	C Sequence analysis of the entire coding region
PCDH15 Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	2	1	D Deletion/duplication analysis
PCDH15 Single Gene Fulgent Genetics United States	3	1	D Deletion/duplication analysis 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
Clinical Exome Fulgent Genetics United States	5128	4672	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Usher Syndrome NGS Panel Fulgent Genetics United States	21	12	D Deletion/duplication analysis C Sequence analysis of the entire coding region
PCDH15 Sequencing Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	3	1	C Sequence analysis of the entire coding region T Targeted variant analysis
Retinitis Pigmentosa NGS Panel Fulgent Genetics United States	329	124	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Eye Disorders NGS Panel Fulgent Genetics United States	1018	459	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Ciliopathies NGS Panel Fulgent Genetics United States	141	97	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Usher Syndrome Panel by next-generation sequencing Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	18	9	C Sequence analysis of the entire coding region
Hereditary Hearing Loss-Common and Non-Syndromic Hearing Loss Panel Genome Diagnostics Laboratory Hospital For Sick Children Canada	64	57	D Deletion/duplication analysis C Sequence analysis of the entire coding region
OtoSeq Hearing Loss Panel by next-generation sequencing (NGS) Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	36	23	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.

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Results: 41 to 58 of 58

Results: 41 to 58 of 58