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Items: 1 to 20 of 338

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv6913713copy number variation1nstd229human GRCh38 chr11: 67,266,401-67,465,100 , GRCh37.p13 chr11: 67,033,872-67,232,571 RNU6-1238P, TMEM134, 16 more genes
    nsv6912757copy number variation1nstd229human GRCh38 chr11: 66,793,001-68,121,500 , GRCh37.p13 chr11: 66,560,472-67,888,967 CHKA-DT, LOC107984341, 66 more genes
    nsv6909452copy number variation1nstd229human GRCh38 chr11: 67,391,601-67,508,800 , GRCh37.p13 chr11: 67,159,072-67,276,271 PPP1CA, TBC1D10C, 14 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6905407copy number variation1nstd229human GRCh38 chr11: 67,371,215-67,371,365 , GRCh37.p13 chr11: 67,138,686-67,138,836 CLCF1, LOC100130987
    nsv6904855copy number variation1nstd229human GRCh38 chr11: 67,331,594-67,339,199 , GRCh37.p13 chr11: 67,099,065-67,106,670 LOC100130987
    nsv6903852copy number variation1nstd229human GRCh38 chr11: 67,378,364-67,380,994 , GRCh37.p13 chr11: 67,145,835-67,148,465 LOC100130987
    nsv6899351copy number variation1nstd229human GRCh38 chr11: 67,385,964-67,388,059 , GRCh37.p13 chr11: 67,153,435-67,155,530 LOC100130987
    nsv6898634copy number variation1nstd229human GRCh38 chr11: 67,266,601-67,521,900 , GRCh37.p13 chr11: 67,034,072-67,289,371 GRK2, CARNS1, 21 more genes
    nsv6595500inversion1nstd223human GRCh38 chr11: 67,359,472-67,360,225 , GRCh37.p13 chr11: 67,126,943-67,127,696 LOC100130987
    nsv6595424inversion1nstd223human GRCh38 chr11: 67,340,592-67,341,382 , GRCh37.p13 chr11: 67,108,063-67,108,853 LOC100130987
    nsv6587895inversion1nstd223human GRCh38 chr11: 67,339,562-67,339,922 , GRCh37.p13 chr11: 67,107,033-67,107,393 LOC100130987
    nsv6473356copy number variation1nstd223human GRCh38 chr11: 67,359,711-67,361,287 , GRCh37.p13 chr11: 67,127,182-67,128,758 RN7SKP239, LOC100130987
    nsv6469652copy number variation1nstd223human GRCh38 chr11: 67,350,574-67,354,288 , GRCh37.p13 chr11: 67,118,045-67,121,759 LOC100130987, POLD4
    nsv6461157copy number variation1nstd223human GRCh38 chr11: 67,327,118-67,328,073 , GRCh37.p13 chr11: 67,094,589-67,095,544 LOC100130987
    nsv6455718copy number variation1nstd223human GRCh38 chr11: 67,385,962-67,388,030 , GRCh37.p13 chr11: 67,153,433-67,155,501 LOC100130987
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6289155insertion1nstd214human GRCh38 chr11: 67,354,230-67,354,230 , GRCh37.p13 chr11: 67,121,701-67,121,701 LOC100130987
    nsv6248161mobile element insertion1nstd215human GRCh38 chr11: 67,380,944-67,380,944 , GRCh37.p13 chr11: 67,148,415-67,148,415 LOC100130987
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