ClinVar Miner

Submissions for variant GRCh37/hg19 22q11.21(chr22:18892575-21460220)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV000767596 SCV000898218 pathogenic Chromosome 22q11.2 microduplication syndrome 2018-11-01 criteria provided, single submitter clinical testing
Baylor Genetics RCV000767687 SCV000898309 pathogenic DiGeorge sequence 2018-11-01 criteria provided, single submitter clinical testing
Baylor Genetics RCV000767692 SCV000898314 pathogenic DiGeorge sequence 2018-11-01 criteria provided, single submitter clinical testing

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