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Items: 1 to 20 of 572

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5932694copy number variation1nstd209human GRCh38 chr18: 12,667,505-12,673,622 , GRCh37.p13 chr18: 12,667,504-12,673,621 PSMG2, CEP76
    nsv5880204copy number variation1nstd209human GRCh38 chr18: 12,661,177-12,663,676 , GRCh37.p13 chr18: 12,661,176-12,663,675 PSMG2, SPIRE1, 1 more genes
    nsv5872231copy number variation1nstd209human GRCh38 chr18: 12,669,730-12,673,879 , GRCh37.p13 chr18: 12,669,729-12,673,878 CEP76, PSMG2
    nsv5702209mobile element insertion1nstd211human GRCh38 chr18: 12,712,371-12,712,371 , GRCh37.p13 chr18: 12,712,370-12,712,370 PSMG2
    nsv5672896copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,656,075-13,885,536 , GRCh38.p12 chr18: 2,656,076-13,885,537 RN7SL862P, LOC105371972, 181 more genes
    nsv5602372copy number variation1nstd207human GRCh38 chr18: 12,669,052-12,669,122 , GRCh37.p13 chr18: 12,669,051-12,669,121 CEP76, PSMG2
    nsv5533147copy number variation1nstd206human GRCh38 chr18: 12,689,183-12,689,307 , GRCh37.p13 chr18: 12,689,182-12,689,306 CEP76, PSMG2
    nsv5532277copy number variation1nstd206human GRCh38 chr18: 12,693,536-12,696,330 , GRCh37.p13 chr18: 12,693,535-12,696,329 PSMG2, CEP76
    nsv5531581copy number variation1nstd206human GRCh38 chr18: 12,715,152-12,716,658 , GRCh37.p13 chr18: 12,715,151-12,716,657 PSMG2
    nsv5519993copy number variation1nstd206human GRCh38 chr18: 12,697,461-12,697,517 , GRCh37.p13 chr18: 12,697,460-12,697,516 PSMG2, CEP76
    nsv5519197copy number variation1nstd206human GRCh38 chr18: 12,677,631-12,677,807 , GRCh37.p13 chr18: 12,677,630-12,677,806 PSMG2, CEP76
    nsv5432330mobile element insertion1nstd206human GRCh38 chr18: 12,712,371-12,712,422 , GRCh37.p13 chr18: 12,712,370-12,712,421 PSMG2
    nsv5152645mobile element insertion1nstd203human GRCh38 chr18: 12,669,933-12,669,953 , GRCh37.p13 chr18: 12,669,932-12,669,952 CEP76, PSMG2
    nsv5026690copy number variation1nstd200human GRCh38 chr18: 12,715,151-12,716,658 , GRCh37.p13 chr18: 12,715,150-12,716,657 PSMG2
    nsv5026689copy number variation1nstd200human GRCh38 chr18: 12,709,234-12,716,593 , GRCh37.p13 chr18: 12,709,233-12,716,592 PSMG2
    nsv5026687copy number variation1nstd200human GRCh38 chr18: 12,651,354-12,656,837 , GRCh37.p13 chr18: 12,651,353-12,656,836 SPIRE1, PSMG2
    nsv5026666copy number variation1nstd200human GRCh38 chr18: 12,045,885-12,921,903 , GRCh37.p13 chr18: 12,045,884-12,921,902 PTPN2, MIX23P3, 25 more genes
    nsv5023945copy number variation1nstd200human GRCh38 chr18: 12,719,130-12,784,116 , GRCh37.p13 chr18: 12,719,129-12,784,115 PTPN2, PSMG2, 1 more genes
    nsv5023944copy number variation1nstd200human GRCh38 chr18: 12,702,436-12,725,766 , GRCh37.p13 chr18: 12,702,435-12,725,765 CEP76, PSMG2
    nsv5014293copy number variation1nstd200human GRCh38 chr18: 12,664,608-12,672,396 , GRCh37.p13 chr18: 12,664,607-12,672,395 CEP76, PSMG2
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