Clinical and research tests for ACTG1 OR ADCY1 OR ATP2B2 OR COL11A2 OR GSDME OR COCH OR DIAPH1 OR EYA4 OR ESRRB OR FOXI1 OR GAB1 OR GJB2 OR GJB3 OR HGF OR KARS1 OR KCNJ10 OR LMX1A OR COX1 OR RNR1 OR TRNS1 OR MYH9 OR MYO6 OR MYO7A OR SLC26A4 OR SERPINB6 OR POU3F4 OR POU4F3 OR RDX OR REST OR SIX1 OR TECTA OR WFS1 OR CLPP OR CDC14A OR KCNQ4 OR S1PR2 OR OTOF OR RIPOR2 OR USH1C OR CIB2 OR GJB6 OR TRIOBP OR P2RX2 OR CLDN14 OR WHRN OR GPSM2 OR MYO15A OR DCDC2 OR MYO3A OR DIABLO OR CDH23 OR TMPRSS3 OR PCDH15 OR MYH14 OR GRHL2 OR ESPN OR TMC1 OR LOXHD1 OR GIPC3 OR OTOA OR CCDC50 OR MARVELD2 OR STRC OR LRTOMT OR LHFPL5 OR SLC17A8 OR MSRB3 OR TMIE OR TPRN OR ILDR1 OR PTPRQ OR SLC26A5 OR GRXCR1 OR MIR96 OR CISD2 OR PJVK - Genetic Testing Registry (GTR)

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Page 1 of 89

Results: 1 to 20 of 1775

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
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
Genomic Unity® Hearing Loss Disorders Analysis Variantyx, Inc. United States	1	318	D Deletion/duplication analysis X Mutation scanning of select exons C Sequence analysis of the entire coding region
Hereditary Hearing Loss and Deafness Panel PreventionGenetics, part of Exact Sciences United States	360	222	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
AudioloGene Hearing Loss Panel Mayo Clinic Laboratories Mayo Clinic United States	1	200	C Sequence analysis of the entire coding region
Hearing loss Panel CGC Genetics Unilabs Portugal	1	277	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
Genomic Unity® Custom Analysis Variantyx, Inc. United States	1	4054	D Deletion/duplication analysis X Mutation scanning of select exons 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
Invitae Comprehensive Deafness Panel Invitae United States	405	219	D Deletion/duplication analysis
Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States	332	167	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hearing Loss Advanced Sequencing and CNV Evaluation Athena Diagnostics United States	248	184	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
Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel Otogenetics United States	123	129	E Sequence analysis of select exons
Inherited Loss of Hearing Panel Dhiti Omics Technologies Private Ltd India	8	179	C Sequence analysis of the entire coding region
Hearing Loss Test GeneDx United States	56	150	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region
Comprehensive Hearing Loss and Deafness Panel Blueprint Genetics Finland	8	179	D Deletion/duplication analysis C Sequence analysis of the entire coding region
OtoGenome Test for Hearing Loss (110 Genes) Laboratory for Molecular Medicine Mass General Brigham Personalized Medicine United States	23	109	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Comprehensive AUDIOME Panel Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States	1	137	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Nonsyndromic Hearing Loss NGS Panel Fulgent Genetics United States	146	99	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hearing Loss Gene Panel Clinical Biochemical Genetics Diagnostic Laboratory University Of Miami Miller School Of Medicine United States	1	136	E Sequence analysis of select exons

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Results: 1 to 20 of 1775

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: 1 to 20 of 1775

Results: 1 to 20 of 1775