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Items: 3

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr17:72916080-72916099
GRCh38:
Chr17:74919985-74920004
USH1GUsher syndrome, type 1G, Usher syndrome, type 1Pathogenic
(Jun 4, 2016)
no assertion criteria provided
2.
GRCh37:
Chr17:72916537
GRCh38:
Chr17:74920442
USH1GUsher syndrome, type 1G, Usher syndrome, type 1Pathogenic
(May 19, 2016)
no assertion criteria provided
3.
GRCh37:
Chr17:72919123
GRCh38:
Chr17:74923028
OTOP2, USH1GUsher syndrome, type 1Likely pathogenic
(May 19, 2016)
no assertion criteria provided
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