ClinVar Miner

Submissions for variant GRCh37/hg19 17p13.2(chr17:3505567-3557452)x1

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories RCV003987207 SCV004802139 pathogenic not specified criteria provided, single submitter clinical testing
Bionano Laboratories RCV000845955 SCV000988076 pathogenic not provided 2017-06-29 no assertion criteria provided clinical testing
Bionano Laboratories RCV000847069 SCV000989191 pathogenic not provided 2018-03-27 no assertion criteria provided clinical testing
Bionano Laboratories RCV000849989 SCV000992131 pathogenic not provided 2017-09-13 no assertion criteria provided clinical testing

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