ClinVar Miner

Submissions for variant NC_000007.13:g.(?_145813093)_(146537016_?)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 RCV000708274 SCV000837384 uncertain significance Cortical dysplasia-focal epilepsy syndrome 2021-03-05 criteria provided, single submitter clinical testing 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. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals with CNTNAP2-related conditions. This variant results in a copy number gain of the genomic region encompassing exon(s) 1-3 of the CNTNAP2 gene. This region includes the initiator codon of the 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 CNTNAP2 gene. As the precise location of this event is unknown, it may be in tandem or it may be located elsewhere in the genome.

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