ClinVar Miner

Submissions for variant GRCh37/hg19 9p24.1-22.1(chr9:4992582-19322101)

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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 RCV002280769 SCV002569036 pathogenic Chromosome 9p deletion syndrome no assertion criteria provided clinical testing

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