ClinVar Miner

Submissions for variant GRCh37/hg19 17p13.2(chr17:3505567-3557441)x1

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories RCV003987205 SCV004802137 pathogenic not specified criteria provided, single submitter clinical testing
Bionano Laboratories RCV000845794 SCV000987915 uncertain significance not provided 2017-07-19 no assertion criteria provided clinical testing
Bionano Laboratories RCV000848322 SCV000990464 pathogenic not provided 2018-02-28 no assertion criteria provided clinical testing
Bionano Laboratories RCV000849845 SCV000991987 pathogenic not provided 2017-12-18 no assertion criteria provided clinical testing
Bionano Laboratories RCV000849925 SCV000992067 pathogenic not provided 2017-10-20 no assertion criteria provided clinical testing

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