ClinVar Miner

Submissions for variant GRCh37/hg19 13q31.3(chr13:92062055-92303438)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 RCV000446126 SCV000501221 uncertain significance See cases no assertion criteria provided clinical testing
ISCA site 1 RCV000510610 SCV000584217 conflicting data from submitters See cases 2016-02-29 no assertion criteria provided clinical testing Uncertain significance(4), Likely benign (3)

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