ClinVar Miner

Submissions for variant NC_000023.10:g.(?_148564277)_(148586667_?)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 RCV003122172 SCV003790856 uncertain significance Mucopolysaccharidosis, MPS-II 2022-10-06 criteria provided, single submitter clinical testing A copy number gain of the genomic region encompassing the full coding sequence of the IDS gene has been identified. The boundaries of this event are unknown as they extend beyond the assayed region for this gene and therefore may encompass additional genes. As the precise location of this event is unknown, it may be in tandem or it may be located elsewhere in the genome. A similar copy number variant has been observed in individual(s) with tetralogy of Fallot (PMID: 22912587). 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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