ClinVar Miner

Submissions for variant GRCh37/hg19 7q11.23(chr7:72717345-74133310)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 RCV001801209 SCV002047421 pathogenic Distal 7q11.23 microdeletion syndrome 2021-10-19 criteria provided, single submitter clinical testing

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