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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074288inversion1nstd229human GRCh38 chr8: 36,881,742-36,938,378 , GRCh37.p13 chr8: 36,739,260-36,795,896 TPT1P8, KCNU1, 1 more genes
    nsv6856124copy number variation1nstd229human GRCh38 chr8: 35,739,256-37,041,962 , GRCh37.p13 chr8: 35,596,774-36,899,480 KCNU1, LOC105379371, 13 more genes
    nsv6852791copy number variation1nstd229human GRCh38 chr8: 36,797,589-37,001,874 , GRCh37.p13 chr8: 36,655,107-36,859,392 TPT1P8, KCNU1, 3 more genes
    nsv6846417copy number variation1nstd229human GRCh38 chr8: 36,583,230-37,073,107 , GRCh37.p13 chr8: 36,440,748-36,930,625 TPT1P8, RNA5SP264, 6 more genes
    nsv6637025copy number variation1nstd102humanPathogenic GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865 LINC02948, LOC105379354, 185 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6574721inversion1nstd223human GRCh38 chr8: 36,881,742-36,938,378 , GRCh37.p13 chr8: 36,739,260-36,795,896 TPT1P8, KCNU1, 1 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6137280copy number variation1nstd213human GRCh37 chr8: 36,090,000-37,220,001 , GRCh38.p12 chr8: 36,232,482-37,362,483 MRPS7P1, RNA5SP264, 14 more genes
    nsv6136576copy number variation1nstd213human GRCh37 chr8: 36,190,000-37,170,001 , GRCh38.p12 chr8: 36,332,482-37,312,483 TPT1P8, KCNU1, 8 more genes
    nsv6136041copy number variation1nstd213human GRCh37 chr8: 36,710,000-37,570,001 , GRCh38.p12 chr8: 36,852,482-37,712,483 SMARCE1P4, LOC100507403, 12 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    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
    nsv4712279copy number variation1nstd195human GRCh38.p12 chr8: 36,832,183-37,193,333 , GRCh37 chr8: 36,689,701-37,050,851 TPT1P8, KCNU1, 5 more genes
    nsv4558818mobile element insertion1nstd166human GRCh37.p13 chr8: 36,746,797-36,746,797 , GRCh38.p12 chr8: 36,889,279-36,889,279 TPT1P8, KCNU1, 1 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456199copy number variation1nstd102humanUncertain significance GRCh37 chr8: 36,094,421-43,822,214 , GRCh38.p12 chr8: 36,236,903-43,967,071 AFG3L2P1, BRF2, 136 more genes
    nsv4436744copy number variation1nstd102humanUncertain significance GRCh37 chr8: 36,486,830-37,992,515 , GRCh38.p12 chr8: 36,629,312-38,134,997 LOC105379380, LOC728024, 29 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
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