ClinVar Miner

Submissions for variant NC_000007.13:g.(?_91851196)_(91852312_?)del

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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 RCV003113956 SCV003795255 likely pathogenic Cerebral cavernous malformation 2022-06-13 criteria provided, single submitter clinical testing In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. A similar copy number variant has been observed in individual(s) with clinical features of cerebral cavernous malformations (Invitae). This variant is a gross deletion of the genomic region encompassing exon(s) 14-15 of the KRIT1 gene. This variant would be expected to be in-frame, preserving the integrity of the reading frame.

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