ClinVar Miner

Submissions for variant NC_000008.11:g.(?_99661334)_(99661511_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000807255 SCV000947298 pathogenic Cohen syndrome 2022-08-28 criteria provided, single submitter clinical testing This variant is a gross deletion of the genomic region encompassing exon(s) 35 of the VPS13B gene. This variant would be expected to be in-frame, preserving the integrity of the reading frame. A similar copy number variant has been observed in individual(s) with VPS13B-related disease (Invitae). In at least one individual the data is consistent with being in trans (on the opposite chromosome) from a pathogenic variant. It has also been observed to segregate with disease in related individuals. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. For these reasons, this variant has been classified as Pathogenic.

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