ClinVar Miner

Submissions for variant GRCh37/hg19 16p12.2(chr16:21801889-22431357)x3

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray,ARUP Laboratories RCV000448291 SCV000502969 uncertain significance See cases no assertion criteria provided clinical testing
ISCA site 1 RCV000511874 SCV000586678 conflicting data from submitters See cases 2016-02-29 no assertion criteria provided clinical testing Uncertain significance(2), Likely benign (1)
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000683789 SCV000811298 uncertain significance not provided 2018-04-24 no assertion criteria provided clinical testing

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