ClinVar Miner

Submissions for variant NC_000017.11:g.(?_31248974)_(31352424_?)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 RCV001032903 SCV001196210 likely pathogenic Neurofibromatosis, type 1 2019-12-11 criteria provided, single submitter clinical testing This variant results in a copy number gain of the genomic region encompassing exons 30-50 of the NF1 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) and may result in an absent or disrupted protein product. This variant has not been reported in the literature in individuals with NF1-related conditions. Loss-of-function variants in NF1 are known to be pathogenic (PMID: 10712197, 23913538). 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.

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