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Items: 1 to 20 of 247

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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
    nsv7071894inversion1nstd229human GRCh38 chr8: 8,228,418-10,333,532 , GRCh37.p13 chr8: 8,085,940-10,191,042 RN7SL178P, LOC107986914, 33 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
    nsv6843294copy number variation1nstd229human GRCh38 chr8: 9,330,677-10,351,763 , GRCh37.p13 chr8: 9,188,187-10,209,273 TNKS, LOC100420404, 11 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
    nsv6634376copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-11,281,408 , GRCh38.p12 chr8: 208,048-11,423,899 DLGAP2-AS1, MIR124-1HG, 228 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6632923copy number variation1nstd224human GRCh37 chr8: 9,472,445-10,090,680 , GRCh38.p12 chr8: 9,614,935-10,233,170 , GRCh38.p12 chr8|NW_018654717.1: 3,114,228-3,736,557 MSRA, TNKS, 5 more genes
    nsv6573530inversion1nstd223human GRCh38 chr8: 9,189,823-13,289,537 , GRCh37.p13 chr8: 9,047,333-13,147,046 MIR1322, LOC105379246, 115 more genes
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