ClinVar Miner

Submissions for variant GRCh37/hg19 1q21.1-21.2(chr1:146043713-147830830)

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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 RCV002280723 SCV002568988 pathogenic Chromosome 1q21.1 duplication syndrome no assertion criteria provided clinical testing

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