ClinVar Miner

Submissions for variant NC_000017.10:g.(?_16842861)_(19578885_?)dup

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003116614 SCV003792821 uncertain significance Immunodeficiency, common variable, 2 2022-08-06 criteria provided, single submitter clinical testing A copy number gain of the genomic region encompassing the full coding sequence of the TNFRSF13B 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 affected with TNFRSF13B-related conditions. 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.
Labcorp Genetics (formerly Invitae), Labcorp RCV003116613 SCV003794101 uncertain significance Familial aplasia of the vermis; Meckel-Gruber syndrome 2022-04-23 criteria provided, single submitter clinical testing A copy number gain of the genomic region encompassing the full coding sequence of the B9D1 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 affected with B9D1-related conditions. 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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