ClinVar Miner

Submissions for variant GRCh37/hg19 13q21.2-21.31(chr13:61660181-63785757)x3

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 1 RCV000512283 SCV000586318 conflicting data from submitters See cases 2016-03-10 no assertion criteria provided clinical testing Uncertain significance(1), Likely benign (1)
Quest Diagnostics Nichols Institute San Juan Capistrano RCV001258551 SCV001435520 likely benign not provided 2019-08-22 no assertion criteria provided clinical testing

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