ClinVar Miner

Submissions for variant GRCh37/hg19 22q11.21(chr22:18916842-20311810)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Rehabilitation Medicine, Incheon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea RCV003319586 SCV004023344 pathogenic Chromosome 22q11.2 microduplication syndrome no assertion criteria provided clinical testing

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