ClinVar Miner

Submissions for variant GRCh37/hg19 15q11.2-13.1(chr15:23620191-28545601)

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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 RCV002280725 SCV002568990 pathogenic 15q11q13 microduplication syndrome no assertion criteria provided clinical testing

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