ClinVar Miner

Submissions for variant GRCh37/hg19 Xq25(chrX:122845829-123288831)

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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 RCV002280687 SCV002568950 pathogenic Xq25 microduplication syndrome no assertion criteria provided clinical testing

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