ClinVar Miner

Submissions for variant GRCh37/hg19 22q11.21(chr22:18937380-21459713)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Shanghai First Maternity and Infant Hospital, Tongji University RCV000788062 SCV000926303 pathogenic Chromosome 22q11.2 microduplication syndrome 2019-03-02 no assertion criteria provided clinical testing

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