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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973938inversion1nstd209human GRCh38 chr8: 41,482,982-43,307,552 , GRCh37.p13 chr8: 41,340,501-43,162,695 , ANK1, 46 more genes
    nsv5917461copy number variation1nstd209human GRCh38 chr8: 41,299,580-47,196,853 , GRCh37.p13 chr8: 41,157,099-48,108,476 , AFG3L2P1, 81 more genes
    nsv5908847copy number variation1nstd209human GRCh38 chr8: 42,249,514-42,257,011 , GRCh37.p13 chr8: 42,107,032-42,114,529 IKBKB-DT
    nsv5867165copy number variation1nstd209human GRCh38 chr8: 42,249,384-42,256,951 , GRCh37.p13 chr8: 42,106,902-42,114,469 IKBKB-DT
    nsv5564499copy number variation1nstd102humanUncertain significance GRCh37 chr8: 41,905,876-42,188,497 , GRCh38.p12 chr8: 42,048,358-42,330,979 LOC101059972, IKBKB-DT, 8 more genes
    nsv5487739copy number variation1nstd206human GRCh38 chr8: 42,267,343-42,268,306 , GRCh37.p13 chr8: 42,124,861-42,125,824 IKBKB-DT
    nsv5481244copy number variation1nstd206human GRCh38 chr8: 42,249,518-42,257,043 , GRCh37.p13 chr8: 42,107,036-42,114,561 IKBKB-DT
    nsv5475903copy number variation1nstd206human GRCh38 chr8: 42,226,318-42,268,730 , GRCh37.p13 chr8: 42,083,836-42,126,248 IKBKB-DT, IKBKB
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5114509mobile element insertion1nstd203human GRCh38 chr8: 42,264,263-42,264,263 , GRCh37.p13 chr8: 42,121,781-42,121,781 IKBKB-DT
    nsv4960394copy number variation1nstd200human GRCh38 chr8: 42,262,988-42,267,921 , GRCh37.p13 chr8: 42,120,506-42,125,439 IKBKB-DT
    nsv4960393copy number variation1nstd200human GRCh38 chr8: 42,257,698-42,260,392 , GRCh37.p13 chr8: 42,115,216-42,117,910 IKBKB-DT
    nsv4960392copy number variation1nstd200human GRCh38 chr8: 42,249,518-42,257,043 , GRCh37.p13 chr8: 42,107,036-42,114,561 IKBKB-DT
    nsv4960391copy number variation1nstd200human GRCh38 chr8: 42,247,767-42,259,386 , GRCh37.p13 chr8: 42,105,285-42,116,904 IKBKB-DT
    nsv4827548copy number variation1nstd200human GRCh37 chr8: 42,107,036-42,114,561 , GRCh38.p12 chr8: 42,249,518-42,257,043 IKBKB-DT
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4715716copy number variation1nstd195human GRCh38.p12 chr8: 41,968,633-42,259,683 , GRCh37 chr8: 41,826,151-42,117,201 PLAT, KAT6A, 6 more genes
    nsv4705434copy number variation1nstd195human GRCh37 chr8: 42,117,251-42,136,501 , GRCh38.p12 chr8: 42,259,733-42,278,983 IKBKB, IKBKB-DT
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
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