ClinVar Miner

Submissions for variant GRCh37/hg19 22q11.21-11.22(chr22:21905051-22989041)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV001801181 SCV002047393 uncertain significance Chromosome 22q11.2 microduplication syndrome 2021-06-28 criteria provided, single submitter clinical testing

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