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Items: 1 to 20 of 261

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7094047copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-9,027,607 , GRCh38.p12 chr12: 4,259,186-8,875,011 ACRBP, OR7E148P, 165 more genes
    nsv7094046copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-5,155,155 , GRCh38.p12 chr12: 4,259,186-5,045,989 RPS15P7, CCND2, 18 more genes
    nsv7076346inversion1nstd229human GRCh38 chr12: 4,815,120-4,815,233 , GRCh37.p13 chr12: 4,924,286-4,924,399 KCNA6
    nsv7073130inversion1nstd229human GRCh38 chr12: 4,823,263-4,833,431 , GRCh37.p13 chr12: 4,932,429-4,942,597 KCNA6
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv7068624inversion1nstd229human GRCh38 chr12: 2,500,360-5,372,895 , GRCh37.p13 chr12: 2,609,526-5,482,061 LOC105369607, IQSEC3P1, 62 more genes
    nsv7064608inversion1nstd229human GRCh38 chr12: 4,844,286-4,844,385 , GRCh37.p13 chr12: 4,953,452-4,953,551 KCNA6
    nsv6938048copy number variation1nstd229human GRCh38 chr12: 4,844,018-4,844,403 , GRCh37.p13 chr12: 4,953,184-4,953,569 KCNA6
    nsv6936832copy number variation1nstd229human GRCh38 chr12: 4,815,850-4,820,341 , GRCh37.p13 chr12: 4,925,016-4,929,507 KCNA6
    nsv6936637copy number variation1nstd229human GRCh38 chr12: 4,814,779-4,850,738 , GRCh37.p13 chr12: 4,923,945-4,959,904 KCNA6
    nsv6931796copy number variation1nstd229human GRCh38 chr12: 4,820,363-4,846,376 , GRCh37.p13 chr12: 4,929,529-4,955,542 KCNA6
    nsv6930965copy number variation1nstd229human GRCh38 chr12: 4,486,494-6,353,198 , GRCh37.p13 chr12: 4,595,660-6,462,364 LOC112268088, NTF3, 34 more genes
    nsv6927801copy number variation1nstd229human GRCh38 chr12: 4,806,001-4,808,700 , GRCh37.p13 chr12: 4,915,167-4,917,866 KCNA6
    nsv6922561copy number variation1nstd229human GRCh38 chr12: 4,816,049-4,816,522 , GRCh37.p13 chr12: 4,925,215-4,925,688 KCNA6
    nsv6918892copy number variation1nstd229human GRCh38 chr12: 4,833,776-4,836,062 , GRCh37.p13 chr12: 4,942,942-4,945,228 KCNA6
    nsv6913746copy number variation1nstd229human GRCh38 chr12: 3,972,756-5,647,610 , GRCh37.p13 chr12: 4,081,922-5,756,776 LOC101901829, LOC100420673, 29 more genes
    nsv6637376copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,787-8,320,544 , GRCh38.p12 chr12: 64,621-8,167,948 GCSHP4, RNU7-1, 220 more genes
    nsv6590771inversion1nstd223human GRCh38 chr12: 4,721,937-5,537,202 , GRCh37.p13 chr12: 4,831,103-5,646,368 KCNA1, KCNA6, 9 more genes
    nsv6588099inversion1nstd223human GRCh38 chr12: 4,823,262-4,833,430 , GRCh37.p13 chr12: 4,932,428-4,942,596 KCNA6
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