ClinVar Miner

Submissions for variant GRCh37/hg19 16p12.2(chr16:21801889-22431357)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Seattle Children's Hospital Molecular Genetics Laboratory, Seattle Children's Hospital RCV002280677 SCV002568940 pathogenic Proximal 16p11.2 microdeletion syndrome no assertion criteria provided clinical testing

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