ClinVar Miner

Submissions for variant GRCh37/hg19 2q32.2-33.1(chr2:190345272-200212289)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medicover Genetics GmbH, Medicover Humangenetik Berlin-Lichtenberg MVZ RCV001255693 SCV001431005 pathogenic Chromosome 2q32-q33 deletion syndrome 2020-07-28 no assertion criteria provided clinical testing PMID: 27774744; PMID: 29023086; PMID: 26811410

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