ClinVar Miner

Submissions for variant GRCh37/hg19 15q13.2-13.3(chr15:31073735-32444044)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 RCV000448974 SCV000501810 pathogenic See cases no assertion criteria provided clinical testing
ISCA site 1 RCV000512233 SCV000584927 uncertain significance See cases 2016-02-11 no assertion criteria provided clinical testing

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