ClinVar Miner

Submissions for variant GRCh37/hg19 9p24.3(chr9:209753-246900)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 RCV003986796 SCV004802925 pathogenic not specified criteria provided, single submitter clinical testing
Bionano Laboratories RCV000847055 SCV000989177 uncertain significance not provided 2018-04-19 no assertion criteria provided clinical testing

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