ClinVar Miner

Submissions for variant GRCh37/hg19 Xp11.22(chrX:53104986-54034505)

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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 RCV002280685 SCV002568948 pathogenic Chromosome Xp11.22 duplication syndrome no assertion criteria provided clinical testing

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