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Items: 1 to 20 of 388

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139986insertion1nstd232human GRCh37.p13 chr2: 10,340,842-10,340,842 , GRCh38.p12 chr2: 10,200,716-10,200,716 RRM2, LOC105373424
    nsv7041767inversion1nstd229human GRCh38 chr2: 7,061,548-10,183,852 , GRCh37.p13 chr2: 7,201,679-10,323,978 LINC00298, KLF11, 52 more genes
    nsv7040494inversion1nstd229human GRCh38 chr2: 10,168,052-10,280,126 , GRCh37.p13 chr2: 10,308,178-10,420,252 RRM2, LOC105373424, 2 more genes
    nsv6676782copy number variation1nstd229human GRCh38 chr2: 10,183,502-10,192,794 , GRCh37.p13 chr2: 10,323,628-10,332,920 RRM2, MIR4261
    nsv6675365copy number variation1nstd229human GRCh38 chr2: 10,128,701-10,133,100 , GRCh37.p13 chr2: 10,268,828-10,273,227 RRM2
    nsv6675279copy number variation1nstd229human GRCh38 chr2: 10,011,501-10,506,700 , GRCh37.p13 chr2: 10,151,628-10,646,826 ODC1, HPCAL1, 11 more genes
    nsv6674963copy number variation1nstd229human GRCh38 chr2: 10,154,801-10,166,428 , GRCh37.p13 chr2: 10,294,928-10,306,554 RRM2
    nsv6674717copy number variation1nstd229human GRCh38 chr2: 10,163,394-10,191,559 , GRCh37.p13 chr2: 10,303,520-10,331,685 MIR4261, RRM2
    nsv6670482copy number variation1nstd229human GRCh38 chr2: 10,109,901-10,128,200 , GRCh37.p13 chr2: 10,250,028-10,268,327 RRM2
    nsv6668479copy number variation1nstd229human GRCh38 chr2: 10,153,149-10,154,139 , GRCh37.p13 chr2: 10,293,276-10,294,266 RRM2
    nsv6668067copy number variation1nstd229human GRCh38 chr2: 10,122,001-10,127,500 , GRCh37.p13 chr2: 10,262,128-10,267,627 RRM2
    nsv6667086copy number variation1nstd229human GRCh38 chr2: 10,047,295-10,133,315 , GRCh37.p13 chr2: 10,187,422-10,273,442 CYS1, RRM2, 1 more genes
    nsv6666576copy number variation1nstd229human GRCh38 chr2: 6,592,339-11,769,396 , GRCh37.p13 chr2: 6,732,471-11,909,522 RN7SKP112, LOC101929861, 103 more genes
    nsv6663823copy number variation1nstd229human GRCh38 chr2: 10,010,915-10,140,233 , GRCh37.p13 chr2: 10,151,042-10,280,360 LOC112268412, KLF11, 3 more genes
    nsv6660579copy number variation1nstd229human GRCh38 chr2: 10,201,233-10,207,381 , GRCh37.p13 chr2: 10,341,359-10,347,507 RRM2, LOC105373424
    nsv6658630copy number variation1nstd229human GRCh38 chr2: 10,187,200-10,248,921 , GRCh37.p13 chr2: 10,327,326-10,389,047 MIR4261, RRM2, 1 more genes
    nsv6636993copy number variation1nstd102humanUncertain significance GRCh37 chr2: 10,192,689-10,462,223 , GRCh38.p12 chr2: 10,052,562-10,322,097 LOC101929691, CYS1, 6 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6543142inversion1nstd223human GRCh38 chr2: 10,154,428-10,154,507 , GRCh37.p13 chr2: 10,294,555-10,294,634 RRM2
    nsv6538197inversion1nstd223human GRCh38 chr2: 10,127,487-10,128,161 , GRCh37.p13 chr2: 10,267,614-10,268,288 RRM2
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