ClinVar Miner

Submissions for variant GRCh37/hg19 16p11.2(chr16:29628661-30306955)

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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 RCV002280688 SCV002568951 pathogenic Chromosome 16p11.2 duplication syndrome no assertion criteria provided clinical testing

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