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Items: 1 to 20 of 277

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148131copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120 XKR6, FAM90A11, 224 more genes
    nsv7148110copy number variation1nstd102humanPathogenic GRCh37 chr8: 7,080,281-12,045,269 , GRCh38.p12 chr8: 7,222,759-12,187,760 DEFB106A, LOC101927997, 176 more genes
    nsv7074774inversion1nstd229human GRCh38 chr8: 7,765,163-10,984,073 , GRCh37.p13 chr8: 7,622,685-10,841,583 PRSS52P, PPP1R3B-DT, 81 more genes
    nsv7069609inversion1nstd229human GRCh38 chr8: 7,102,414-12,683,056 , GRCh37.p13 chr8: 6,959,936-12,540,565 FAM90A20, LOC107986910, 201 more genes
    nsv7067997inversion1nstd229human GRCh38 chr8: 8,181,479-12,388,066 , GRCh37.p13 chr8: 8,039,001-12,245,575 TNKS, ZNF705D, 113 more genes
    nsv7065354inversion1nstd229human GRCh38 chr8: 9,129,798-15,405,439 , GRCh37.p13 chr8: 8,987,308-15,262,948 FAM167A, LOC729732, 132 more genes
    nsv7062538inversion1nstd229human GRCh38 chr8: 7,137,678-12,551,118 , GRCh37.p13 chr8: 6,995,200-12,408,627 MIR124-1, MFHAS1, 197 more genes
    nsv7060774inversion1nstd229human GRCh38 chr8: 7,366,932-11,853,836 , GRCh37.p13 chr8: 7,224,454-11,711,345 DEFB104B, SNORA99, 135 more genes
    nsv7059146inversion1nstd229human GRCh38 chr8: 7,352,588-12,547,775 , GRCh37.p13 chr8: 7,210,110-12,405,284 LOC107986910, HSPD1P2, 179 more genes
    nsv7058956inversion1nstd229human GRCh38 chr8: 8,224,000-12,734,745 , GRCh37.p13 chr8: 8,081,522-12,592,254 MIR3926-1, FAM90A25P, 129 more genes
    nsv6856759copy number variation1nstd229human GRCh38 chr8: 10,731,275-10,947,447 , GRCh37.p13 chr8: 10,588,785-10,804,957 MIR1322, PINX1-DT, 5 more genes
    nsv6852959copy number variation1nstd229human GRCh38 chr8: 10,751,889-10,847,667 , GRCh37.p13 chr8: 10,609,399-10,705,177 LOC102723313, PINX1, 2 more genes
    nsv6852841copy number variation1nstd229human GRCh38 chr8: 10,765,483-11,438,758 , GRCh37.p13 chr8: 10,622,993-11,296,267 LOC101929269, RPL19P13, 18 more genes
    nsv6852428copy number variation1nstd229human GRCh38 chr8: 10,792,792-10,862,284 , GRCh37.p13 chr8: 10,650,302-10,719,794 PINX1-DT, MIR1322, 3 more genes
    nsv6838698copy number variation1nstd229human GRCh38 chr8: 10,823,168-10,835,858 , GRCh37.p13 chr8: 10,680,678-10,693,368 MIR1322, PINX1
    nsv6838527copy number variation1nstd229human GRCh38 chr8: 10,810,401-11,158,500 , GRCh37.p13 chr8: 10,667,911-11,016,010 LOC101929269, PINX1-DT, 6 more genes
    nsv6636968copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-18,936,715 , GRCh38.p12 chr8: 208,049-19,079,205 ZNF705B, NATP, 357 more genes
    nsv6636940copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-10,965,627 , GRCh38.p12 chr8|NW_018654717.1: 1-5,513,617 , GRCh38.p12 chr8: 208,049-11,108,117 HSPD1P3, LOC401442, 270 more genes
    nsv6636617copy number variation1nstd102humanPathogenic GRCh37 chr8: 8,093,066-12,548,732 , GRCh38.p12 chr8: 8,235,544-12,691,223 , GRCh38.p12 chr8|NW_018654717.1: 996,517-5,112,321 DEFB131D, RNU6-682P, 128 more genes
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