ClinVar Miner

Submissions for variant NC_000023.10:g.(?_31222078)_(31241238_?)dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000708513 SCV000837623 pathogenic Duchenne muscular dystrophy 2017-08-01 criteria provided, single submitter clinical testing This variant is a gross duplication of the genomic region encompassing exons 64-67 of the DMD gene. While the exact position of the duplicated exons cannot be determined from this data, the duplicated copy of this region is likely in tandem and may result in an absent or disrupted protein product. This variant has been reported in an individual with Becker muscular dystrophy (PMID: 17253928) and Duchenne muscular dystrophy (PMID: 17561468), as well as a carrier female (PMID: 17854090). Sub-genic duplications are generally in tandem (PMID: 25640679), and result in an absent or disrupted protein. Loss-of-function variants in DMD are known to be pathogenic (PMID: 16770791, 25007885). For these reasons, this variant has been classified as Pathogenic.

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