ClinVar Miner

Submissions for variant NC_000001.10:g.(?_237893550)_(237995957_?)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 RCV000804612 SCV000944529 uncertain significance Catecholaminergic polymorphic ventricular tachycardia 2018-10-31 criteria provided, single submitter clinical testing This variant results in a copy number gain of the genomic region encompassing exons 77-105 of the RYR2 gene. The 5' boundary is likely confined to intron 76. The 3' end of this event is unknown as it extends 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 RYR2-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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