ClinVar Miner

Submissions for variant GRCh37/hg19 16p13.11(chr16:16247252-16262036)x1

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories RCV003987135 SCV004802067 pathogenic not specified criteria provided, single submitter clinical testing
Bionano Laboratories RCV000849654 SCV000991796 pathogenic not provided 2018-02-16 no assertion criteria provided clinical testing

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