ClinVar Miner

Submissions for variant GRCh37/hg19 16p13.11(chr16:14866283-16544419)x3

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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 RCV003987170 SCV004802102 pathogenic not specified criteria provided, single submitter clinical testing
ISCA site 1 RCV000511683 SCV000586220 uncertain significance See cases 2015-08-12 no assertion criteria provided clinical testing

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