ClinVar Miner

Submissions for variant GRCh37/hg19 6p11.2-q11.1(chr6:57590853-62891976)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Cytogenetics Laboratory, University of Washington RCV000184093 SCV000236627 likely benign See cases 2015-05-28 criteria provided, single submitter clinical testing

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