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| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel Otogenetics United States | 123 | 129 |
|
TECTA - NGS including CNV analysis Centogene US, LLC - The Rare Disease Company United States | 2 | 1 |
|
TECTA - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
|
Invitae Comprehensive Deafness Panel Invitae United States | 405 | 219 |
|
Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 288 | 218 |
|
Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
Hereditary Hearing Loss and Deafness Panel PreventionGenetics United States | 356 | 209 |
|
PreventionGenetics United States | 2 | 1 |
|
GJB2. Detection of the mutation c.35delG by sequencing IGENOMIX Spain | 3 | 1 |
|
IGENOMIX Spain | 3 | 1 |
|
IGENOMIX Spain | 3 | 1 |
|
IGENOMIX Spain | 3 | 1 |
|
GJB2 (Conexina 26). Detection of the mutation c.35delG by sequencing IGENOMIX Spain | 3 | 1 |
|
GJB2 (Conexina 26). Complete sequencing IGENOMIX Spain | 3 | 1 |
|
Autosomal Dominant Hearing Loss. 25-gene NGS panel. Genologica Medica Spain | 48 | 23 |
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Non-syndromic hearing loss panel. 95-gene NGS panel. Genologica Medica Spain | 146 | 94 |
|
Autosomal recessive hearing loss. 41-gene NGS panel. Genologica Medica Spain | 65 | 41 |
|
Deafness, autosomal dominant 12 (sequence analysis of TECTA gene) Unilabs Genetics CGC Genetics Portugal | 2 | 1 |
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Non syndromic deafness (deletion/dplucation analysis on TECTA gene) Unilabs Genetics CGC Genetics Portugal | 2 | 1 |
|
Hearing Loss, Comprehensive Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 142 | 84 |
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