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Items: 1 to 20 of 548

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5672526copy number variation1nstd102humanPathogenic GRCh37 chr10: 127,548,166-135,440,251 , GRCh38.p12 chr10: 125,859,597-133,626,747 LINC00601, RPL5P28, 110 more genes
    nsv5662376insertion2nstd207human GRCh38 chr10: 133,265,181-133,265,181 , GRCh37.p13 chr10: 135,078,685-135,078,685 ADAM8
    nsv5651645insertion1nstd207human GRCh38 chr10: 133,265,103-133,265,103 , GRCh37.p13 chr10: 135,078,607-135,078,607 ADAM8
    nsv5591796copy number variation1nstd207human GRCh38 chr10: 133,262,014-133,262,064 , GRCh37.p13 chr10: 135,075,518-135,075,568 ADAM8
    nsv5589470copy number variation1nstd207human GRCh38 chr10: 133,264,903-133,265,180 , GRCh37.p13 chr10: 135,078,407-135,078,684 ADAM8
    nsv5585622copy number variation1nstd207human GRCh38 chr10: 133,264,829-133,264,947 , GRCh37.p13 chr10: 135,078,333-135,078,451 ADAM8
    nsv5504019copy number variation1nstd206human GRCh38 chr10: 133,200,862-133,379,746 , GRCh37.p13 chr10: 135,014,366-135,193,250 MIR202HG, VENTX, 14 more genes
    nsv5502802copy number variation1nstd206human GRCh38 chr10: 133,271,285-133,271,357 , GRCh37.p13 chr10: 135,084,789-135,084,861 ADAM8
    nsv5381769copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,483,682-135,434,178 , GRCh38.p12 chr10: 127,685,418-133,620,674 DPYSL4, LINC02667, 88 more genes
    nsv5354635translocation1nstd200human GRCh38 chr10: 133,268,574-133,268,574 , GRCh38 chr10: 133,268,158-133,268,158 , GRCh37.p13 chr10: 135,081,662-135,081,662 , GRCh37.p13 chr10: 135,082,078-135,082,078 ADAM8
    nsv5251079copy number variation1nstd204human GRCh38.p13 chr10: 133,252,174-133,298,999 , GRCh37.p13 chr10: 135,065,678-135,112,503 ADAM8, TUBGCP2
    nsv4984073copy number variation1nstd200human GRCh38 chr10: 133,267,728-133,297,904 , GRCh37.p13 chr10: 135,081,232-135,111,408 TUBGCP2, ADAM8
    nsv4984060copy number variation1nstd200human GRCh38 chr10: 132,934,989-133,515,554 , GRCh37.p13 chr10: 134,748,493-135,329,058 , SCART1, 33 more genes
    nsv4977735copy number variation1nstd200human GRCh38 chr10: 133,273,395-133,273,470 , GRCh37.p13 chr10: 135,086,899-135,086,974 ADAM8
    nsv4846352copy number variation1nstd200human GRCh37 chr10: 135,081,662-135,082,078 , GRCh38.p12 chr10: 133,268,158-133,268,574 ADAM8
    nsv4839612copy number variation1nstd200human GRCh37 chr10: 135,081,232-135,111,408 , GRCh38.p12 chr10: 133,267,728-133,297,904 TUBGCP2, ADAM8
    nsv4832477copy number variation1nstd200human GRCh37 chr10: 135,074,480-135,074,879 , GRCh38.p12 chr10: 133,260,976-133,261,375 ADAM8
    nsv4733721copy number variation1nstd199human GRCh37 chr10: 135,078,487-135,078,646 , GRCh38.p12 chr10: 133,264,983-133,265,142 ADAM8
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