ClinVar Miner

Submissions for variant GRCh37/hg19 13q12.11(chr13:20796981-21104487)x1

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Total submissions: 10
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories RCV003987007 SCV004803136 pathogenic not specified criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000683514 SCV000811023 uncertain significance not provided 2019-03-27 no assertion criteria provided clinical testing
Bionano Laboratories RCV000845836 SCV000987957 uncertain significance not provided 2017-11-20 no assertion criteria provided clinical testing
Bionano Laboratories RCV000846003 SCV000988124 uncertain significance not provided 2018-06-07 no assertion criteria provided clinical testing
Bionano Laboratories RCV000846146 SCV000988267 uncertain significance not provided 2018-04-05 no assertion criteria provided clinical testing
Bionano Laboratories RCV000846310 SCV000988431 uncertain significance not provided 2017-11-29 no assertion criteria provided clinical testing
Bionano Laboratories RCV000846547 SCV000988669 uncertain significance not provided 2018-03-06 no assertion criteria provided clinical testing
Bionano Laboratories RCV000848101 SCV000990234 uncertain significance not provided 2018-06-19 no assertion criteria provided clinical testing
Bionano Laboratories RCV000849187 SCV000991329 uncertain significance not provided 2017-10-26 no assertion criteria provided clinical testing
Bionano Laboratories RCV000849987 SCV000992129 uncertain significance not provided 2018-04-17 no assertion criteria provided clinical testing

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