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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
    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
    nsv6852960copy number variation1nstd229human GRCh38 chr8: 11,295,328-11,297,720 , GRCh37.p13 chr8: 11,152,837-11,155,229 MTMR9
    nsv6852874copy number variation1nstd229human GRCh38 chr8: 11,207,014-11,457,418 , GRCh37.p13 chr8: 11,064,523-11,314,927 RPL19P13, TDH-AS1, 8 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
    nsv6844575copy number variation1nstd229human GRCh38 chr8: 10,984,101-11,398,800 , GRCh37.p13 chr8: 10,841,611-11,256,309 LOC101929290, FAM167A-AS1, 11 more genes
    nsv6844204copy number variation1nstd229human GRCh38 chr8: 11,323,630-11,324,126 , GRCh37.p13 chr8: 11,181,139-11,181,635 LOC101929290, MTMR9
    nsv6842516copy number variation1nstd229human GRCh38 chr8: 11,294,728-11,294,773 , GRCh37.p13 chr8: 11,152,237-11,152,282 MTMR9
    nsv6842312copy number variation1nstd229human GRCh38 chr8: 11,300,979-11,304,361 , GRCh37.p13 chr8: 11,158,488-11,161,870 MTMR9
    nsv6838159copy number variation1nstd229human GRCh38 chr8: 11,236,895-11,301,870 , GRCh37.p13 chr8: 11,094,404-11,159,379 RPL19P13, MTMR9
    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
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