ClinVar Miner

Submissions for variant NC_000008.10:g.(?_11560787)_(11616004_?)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 RCV000556918 SCV000651993 uncertain significance Atrioventricular septal defect 4 2017-05-23 criteria provided, single submitter clinical testing A gross duplication of the genomic region encompassing the full coding sequence of the GATA4 gene has been identified. The boundaries of this event are unknown as the duplication extends beyond the assayed region for this gene and therefore may encompass additional genes. As the precise location of this duplication is unknown, it may be in tandem or it may be located elsewhere in the genome. Gross duplications confined to the GATA4 gene have not been reported previously in the literature. The exact genomic location of this variant is unknown. In summary, this duplication has uncertain impact on GATA4 function. The available evidence is currently insufficient to determine its role in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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