ClinVar Miner

Submissions for variant NC_000022.11:g.(?_19755901)_(19783042_?)del

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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 RCV000707894 SCV000837004 pathogenic DiGeorge syndrome 2019-12-23 criteria provided, single submitter clinical testing A gross deletion of the genomic region encompassing the full coding sequence of the TBX1 gene has been identified. The boundaries of this event are unknown as the deletion extends beyond the assayed region for this gene and therefore may encompass additional genes. Contiguous gene deletions that include TBX1 have been observed in multiple individuals with congenital heart disease, DiGeorge syndrome, and pulmonary atresia (PMID: 25205790, 25516202, 24826987). Loss-of-function variants in TBX1 are known to be pathogenic (PMID: 11239417, 11242049). For these reasons, this variant has been classified as Pathogenic.

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