ClinVar Miner

Submissions for variant GRCh38/hg38 16p12.2(chr16:21825971-22396751)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 RCV000148152 SCV000077777 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 17 RCV000050457 SCV000175192 benign See cases 2009-07-30 no assertion criteria provided clinical testing

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