ClinVar Miner

Submissions for variant NC_000005.10:g.(177090796_177094455)_(177346090_177352856)dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre of Medical Genetics, University of Antwerp RCV001199823 SCV001190345 pathogenic 5q35 microduplication syndrome 2019-12-16 criteria provided, single submitter research

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