ClinVar Miner

Submissions for variant NC_000004.11:g.(?_493105)_(499736_?)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 RCV000708202 SCV000837312 uncertain significance Intellectual disability, autosomal recessive 53 2019-06-18 criteria provided, single submitter clinical testing This variant results in a copy number gain of the genomic region encompassing exons 1-3 of the PIGG gene. The 5' end of this event is unknown as it extends beyond the assayed region for this gene and therefore may encompass additional genes. The 3' boundary is likely confined to intron 3 of the PIGG gene. 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 PIGG-related disease. 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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