ClinVar Miner

Submissions for variant NC_000008.10:g.(100568882_100587885)_(100789185_100790909)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004766527 SCV005381223 pathogenic Cohen syndrome 2024-08-07 criteria provided, single submitter clinical testing Variant summary: The variant involves the deletion of exons 32-41 in the VPS13B gene. A presumed nomenclature of c.(5024+1_5025-1)_(7504+1_7505-1)del has been designated for the purposes of this classification. This Copy Number Variant (CNV) is expected to alter the reading frame and predicted to result in a truncation or absence of the encoded protein due to nonsense mediated decay (NMD). The variant was absent in 21694 control chromosomes. To our knowledge, no occurrence of c.(5024+1_5025-1)_(7504+1_7505-1)del in individuals affected with Cohen Syndrome and no experimental evidence demonstrating its impact on protein function have been reported. No submitters have cited clinical-significance assessments for this variant to ClinVar. Based on the evidence outlined above, the variant was classified as pathogenic.

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