ClinVar Miner

Submissions for variant NC_000008.11:g.(?_99766774)_(99784476_?)dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001033617 SCV001196924 uncertain significance Cohen syndrome 2020-10-01 criteria provided, single submitter clinical testing This variant results in a copy number gain of the genomic region encompassing exons 40-43 of the VPS13B gene. While the exact position of this variant cannot be determined from this data, sub-genic copy number gains are generally in tandem (PMID: 25640679). This variant would be expected to be in-frame, preserving the integrity of the reading frame. This variant has not been reported in the literature in individuals with VPS13B-related conditions. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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