| | LOC121466733, LOC121468000 +2048 more | Copy number loss | See cases | |
| | LOC130010147, LOC130010148 +2049 more | Copy number gain | See cases | |
| | LOC130009360, LOC130009361 +2047 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130009909, LOC130009910 +2044 more | Copy number gain | See cases | |
| | LINC00333, LINC00343 +2045 more | Copy number gain | See cases | |
| | CRYL1, EEF1AKMT1 +116 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC112163664, LOC112163665 +2040 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC121838573, LOC121838574 +2028 more | Copy number gain | See cases | |
| | LOC130009528, LOC130009529 +620 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LINC00462, LINC00463 +2021 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Duplication | Autosomal recessive nonsyndromic hearing loss 1B +3 more | |
| | | Copy number loss | See cases | |
| | | Single nucleotide variant | Nonsyndromic Hearing Loss, Dominant +4 more | |
| | | Deletion (3 prime UTR variant) | Keratitis ichthyosis and deafness syndrome +4 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 1A +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal dominant nonsyndromic hearing loss 3A +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 1A +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Knuckle pads, deafness AND leukonychia syndrome +7 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Palmoplantar keratoderma-deafness syndrome +8 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal dominant nonsyndromic hearing loss 3A +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Single nucleotide variant (missense variant) | not specified +9 more | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Single nucleotide variant (missense variant) | Mutilating keratoderma +9 more | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Deletion | Hearing impairment +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Hearing loss | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Deletion (frameshift variant) | Rare genetic deafness +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Microsatellite (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +12 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +10 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Duplication (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Indel | not provided | |
| | | Indel | Rare genetic deafness +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |