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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056404inversion1nstd229human GRCh38 chr7: 45,643,008-53,582,757 , GRCh37.p13 chr7: 45,682,607-53,650,450 PKD1L1, FIGNL1, 79 more genes
    nsv7054715inversion1nstd229human GRCh38 chr7: 45,763,995-45,774,495 , GRCh37.p13 chr7: 45,803,594-45,814,094 GTF2IP13, SEPTIN7P2
    nsv7050870inversion1nstd229human GRCh38 chr7: 45,735,362-45,735,608 , GRCh37.p13 chr7: 45,774,961-45,775,207 SEPTIN7P2
    nsv7046943inversion1nstd229human GRCh38 chr7: 45,642,996-53,582,758 , GRCh37.p13 chr7: 45,682,595-53,650,451 CDC14C, ROBO2P1, 79 more genes
    nsv7039894inversion1nstd229human GRCh38 chr7: 45,735,605-45,736,990 , GRCh37.p13 chr7: 45,775,204-45,776,589 SEPTIN7P2
    nsv6834090copy number variation1nstd229human GRCh38 chr7: 45,746,055-45,748,111 , GRCh37.p13 chr7: 45,785,654-45,787,710 SEPTIN7P2
    nsv6823610copy number variation1nstd229human GRCh38 chr7: 45,750,434-45,755,813 , GRCh37.p13 chr7: 45,790,033-45,795,412 SEPTIN7P2
    nsv6821384copy number variation1nstd229human GRCh38 chr7: 45,749,001-45,749,060 , GRCh37.p13 chr7: 45,788,600-45,788,659 SEPTIN7P2
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6613896copy number variation1nstd223human GRCh38 chr7: 45,730,517-45,741,460 , GRCh37.p13 chr7: 45,770,116-45,781,059 SEPTIN7P2
    nsv6612030copy number variation1nstd223human GRCh38 chr7: 45,726,201-45,731,600 , GRCh37.p13 chr7: 45,765,800-45,771,199 SEPTIN7P2
    nsv6603456copy number variation1nstd223human GRCh38 chr7: 45,748,001-45,748,900 , GRCh37.p13 chr7: 45,787,600-45,788,499 SEPTIN7P2
    nsv6602908copy number variation1nstd223human GRCh38 chr7: 45,736,215-45,736,595 , GRCh37.p13 chr7: 45,775,814-45,776,194 SEPTIN7P2
    nsv6574607inversion1nstd223human GRCh38 chr7: 35,958,610-45,735,691 , GRCh37.p13 chr7: 35,998,220-45,775,290 RPS17P13, LOC105375252, 182 more genes
    nsv6572893inversion1nstd223human GRCh38 chr7: 45,642,996-53,582,758 , GRCh37.p13 chr7: 45,682,595-53,650,451 LOC730234, LOC105375278, 79 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313509copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,778,439-50,228,656 , GRCh38.p12 chr7: 40,738,840-50,189,060 LINC01447, ABCA13, 142 more genes
    nsv6308297mobile element insertion1nstd186human GRCh37 chr7: 45,787,949-45,788,000 , GRCh38.p12 chr7: 45,748,350-45,748,401 SEPTIN7P2
    nsv6301456copy number variation1nstd186human GRCh37 chr7: 45,793,956-45,794,253 , GRCh38.p12 chr7: 45,754,357-45,754,654 SEPTIN7P2
    nsv6239385mobile element insertion1nstd215human GRCh38 chr7: 45,758,407-45,758,407 , GRCh37.p13 chr7: 45,798,006-45,798,006 SEPTIN7P2
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