ClinVar Miner

Submissions for variant GRCh37/hg19 8p23.1(chr8:7080281-12045269)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 RCV003329529 SCV004036114 pathogenic 8p23.1 duplication syndrome 2022-11-17 criteria provided, single submitter clinical testing

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