ClinVar Miner

Submissions for variant GRCh37/hg19 13q31.1(chr13:85812936-86436723)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 RCV003987004 SCV004803133 pathogenic not specified criteria provided, single submitter clinical testing
Bionano Laboratories RCV000847517 SCV000989639 uncertain significance not provided 2017-11-21 no assertion criteria provided clinical testing

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