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Items: 1 to 20 of 269

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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
    nsv7071529inversion1nstd229human GRCh38 chr8: 10,617,803-10,694,594 , GRCh37.p13 chr8: 10,475,313-10,552,104 MIR4286, RNA5SP252, 2 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
    nsv6857352copy number variation1nstd229human GRCh38 chr8: 10,121,278-10,725,166 , GRCh37.p13 chr8: 9,978,788-10,582,676 LINC03022, SOX7, 10 more genes
    nsv6849332copy number variation1nstd229human GRCh38 chr8: 10,206,220-10,704,841 , GRCh37.p13 chr8: 10,063,730-10,562,351 LOC105379237, RNU6-729P, 9 more genes
    nsv6848767copy number variation1nstd229human GRCh38 chr8: 10,094,505-10,720,921 , GRCh37.p13 chr8: 9,952,015-10,578,431 RNU6-729P, PRSS55, 9 more genes
    nsv6844836copy number variation1nstd229human GRCh38 chr8: 10,024,094-10,673,120 , GRCh37.p13 chr8: 9,881,604-10,530,630 PRSS52P, LOC100420053, 9 more genes
    nsv6839322copy number variation1nstd229human GRCh38 chr8: 10,358,072-10,697,935 , GRCh37.p13 chr8: 10,215,582-10,555,445 C8orf74, MSRA, 8 more genes
    nsv6838610copy number variation1nstd229human GRCh38 chr8: 10,666,415-10,672,163 , GRCh37.p13 chr8: 10,523,925-10,529,673 C8orf74, MIR4286
    nsv6838125copy number variation1nstd229human GRCh38 chr8: 10,617,801-10,701,200 , GRCh37.p13 chr8: 10,475,311-10,558,710 RP1L1, C8orf74, 2 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
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