ClinVar Miner

Submissions for variant NC_000005.10:g.(?_128301372)_(128312805_?)dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001032337 SCV001195644 uncertain significance Congenital contractural arachnodactyly 2019-01-30 criteria provided, single submitter clinical testing This variant results in a copy number gain of the genomic region encompassing exons 37-47 of the FBN2 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 been observed in an individual affected with clinical features of congenital contractural arachnodactyly (Invitae). 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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