ClinVar Miner

Submissions for variant NC_000023.10:g.(?_118968821)_(118986911_?)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 RCV001958231 SCV002222971 uncertain significance Syndromic X-linked intellectual disability 14 2021-06-05 criteria provided, single submitter clinical testing A copy number gain of the genomic region encompassing the full coding sequence of the UPF3B gene has been identified. The boundaries of this event are unknown as they extend beyond the assayed region for this gene and therefore may encompass additional genes. As the precise location of this event is unknown, it may be in tandem or it may be located elsewhere in the genome. This variant has not been reported in the literature in individuals with UPF3B-related conditions. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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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