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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121607copy number variation1nstd186human GRCh37 chr12: 51,473,405-51,473,786 , GRCh38.p12 chr12: 51,079,622-51,080,003 CSRNP2
    nsv5704821mobile element insertion2nstd211human GRCh38 chr12: 51,076,835-51,076,835 , GRCh37.p13 chr12: 51,470,618-51,470,618 CSRNP2
    nsv5661679insertion1nstd207human GRCh38 chr12: 51,079,769-51,079,769 , GRCh37.p13 chr12: 51,473,552-51,473,552 CSRNP2
    nsv5600606copy number variation1nstd207human GRCh38 chr12: 51,069,350-51,069,755 , GRCh37.p13 chr12: 51,463,133-51,463,538 LETMD1, CSRNP2
    nsv5556240sequence alteration1nstd206human GRCh38 chr12: 50,501,429-51,116,796 , GRCh37.p13 chr12: 50,895,212-51,510,579 ATF1, SLC11A2, 14 more genes
    nsv5500359copy number variation1nstd206human GRCh38 chr12: 51,035,633-51,071,431 , GRCh37.p13 chr12: 51,429,416-51,465,214 CSRNP2, RNU6-1273P, 1 more genes
    nsv5498467copy number variation1nstd206human GRCh38 chr12: 51,079,622-51,080,003 , GRCh37.p13 chr12: 51,473,405-51,473,786 CSRNP2
    nsv5422062mobile element insertion1nstd206human GRCh38 chr12: 51,076,835-51,076,886 , GRCh37.p13 chr12: 51,470,618-51,470,669 CSRNP2
    nsv5391614copy number variation1nstd186human GRCh37 chr12: 51,463,175-51,463,539 , GRCh38.p12 chr12: 51,069,392-51,069,756 CSRNP2, LETMD1
    nsv5391260copy number variation1nstd186human GRCh37 chr12: 51,463,159-51,463,544 , GRCh38.p12 chr12: 51,069,376-51,069,761 CSRNP2, LETMD1
    nsv5390272copy number variation1nstd186human GRCh37 chr12: 51,473,404-51,473,791 , GRCh38.p12 chr12: 51,079,621-51,080,008 CSRNP2
    nsv5311479copy number variation1nstd204human GRCh37.p13 chr12: 51,463,054-51,463,568 , GRCh38.p13 chr12: 51,069,271-51,069,785 CSRNP2, LETMD1
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv4972658copy number variation1nstd200human GRCh38 chr12: 51,072,549-51,073,716 , GRCh37.p13 chr12: 51,466,332-51,467,499 CSRNP2
    nsv4972657copy number variation1nstd200human GRCh38 chr12: 51,069,376-51,069,761 , GRCh37.p13 chr12: 51,463,159-51,463,544 LETMD1, CSRNP2
    nsv4840079copy number variation1nstd200human GRCh37 chr12: 51,463,174-51,463,539 , GRCh38.p12 chr12: 51,069,391-51,069,756 LETMD1, CSRNP2
    nsv4830946copy number variation1nstd200human GRCh37 chr12: 51,473,393-51,473,810 , GRCh38.p12 chr12: 51,079,610-51,080,027 CSRNP2
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
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