ClinVar Miner

Submissions for variant NC_000011.9:g.(?_68582782)_(68582962_?)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 RCV003107528 SCV003794513 uncertain significance Carnitine palmitoyl transferase 1A deficiency 2019-11-11 criteria provided, single submitter clinical testing This variant results in a copy number gain of the genomic region encompassing exon 2 of the CPT1A gene, which includes the initiator codon. 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 2 of the CPT1A gene. 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 CPT1A-related conditions. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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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