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Items: 1 to 20 of 538

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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
    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
    nsv7097783copy number variation1nstd102humanUncertain significance GRCh37 chr8: 11,408,516-11,412,378 , GRCh38.p12 chr8: 11,551,007-11,554,869 , GRCh38.p12 chr8|NW_018654717.1: 1,793,229-1,797,091 BLK, LOC105379241
    nsv7070191inversion1nstd229human GRCh38 chr8: 11,431,142-11,714,759 , GRCh37.p13 chr8: 11,288,651-11,572,268 BLK, GATA4, 6 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
    nsv7065369inversion1nstd229human GRCh38 chr8: 11,532,884-11,552,609 , GRCh37.p13 chr8: 11,390,393-11,410,118 BLK, LOC105379241
    nsv7065354inversion1nstd229human GRCh38 chr8: 9,129,798-15,405,439 , GRCh37.p13 chr8: 8,987,308-15,262,948 FAM167A, LOC729732, 132 more genes
    nsv7062682inversion1nstd229human GRCh38 chr8: 11,486,499-11,539,366 , GRCh37.p13 chr8: 11,344,008-11,396,875 BLK
    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
    nsv6857849copy number variation1nstd229human GRCh38 chr8: 11,526,555-11,535,005 , GRCh37.p13 chr8: 11,384,064-11,392,514 BLK
    nsv6857758copy number variation1nstd229human GRCh38 chr8: 11,557,711-11,560,933 , GRCh37.p13 chr8: 11,415,220-11,418,442 BLK
    nsv6856903copy number variation1nstd229human GRCh38 chr8: 11,500,355-11,528,217 , GRCh37.p13 chr8: 11,357,864-11,385,726 BLK
    nsv6855675copy number variation1nstd229human GRCh38 chr8: 11,528,865-11,531,108 , GRCh37.p13 chr8: 11,386,374-11,388,617 BLK
    nsv6853760copy number variation1nstd229human GRCh38 chr8: 11,531,738-11,611,042 , GRCh37.p13 chr8: 11,389,247-11,468,551 LINC00208, BLK, 1 more genes
    nsv6853599copy number variation1nstd229human GRCh38 chr8: 11,546,521-11,546,834 , GRCh37.p13 chr8: 11,404,030-11,404,343 BLK
    nsv6850275copy number variation1nstd229human GRCh38 chr8: 11,524,604-11,528,220 , GRCh37.p13 chr8: 11,382,113-11,385,729 BLK
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