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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5657553insertion1nstd207human GRCh38 chr12: 64,204,048-64,204,048 , GRCh37.p13 chr12: 64,597,828-64,597,828 KICS2, RNU6-1009P
    nsv5316266copy number variation1nstd204human GRCh38.p13 chr12: 64,202,479-64,227,215 , GRCh37.p13 chr12: 64,596,259-64,620,995 RNU5A-7P, KICS2, 1 more genes
    nsv5278616copy number variation1nstd204human GRCh38.p13 chr12: 64,202,280-64,226,319 , GRCh37.p13 chr12: 64,596,060-64,620,099 KICS2, RNU6-1009P
    nsv5261225copy number variation1nstd204human GRCh38.p13 chr12: 64,201,101-64,226,400 , GRCh37.p13 chr12: 64,594,881-64,620,180 KICS2, RNU6-1009P
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv5008581copy number variation1nstd200human GRCh38 chr12: 64,202,489-64,227,206 , GRCh37.p13 chr12: 64,596,269-64,620,986 RNU5A-7P, KICS2, 1 more genes
    nsv4994976copy number variation1nstd200human GRCh38 chr12: 64,179,725-64,210,120 , GRCh37.p13 chr12: 64,573,505-64,603,900 KICS2, RNU6-1009P
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4848643copy number variation1nstd200human GRCh37 chr12: 64,596,269-64,620,986 , GRCh38.p12 chr12: 64,202,489-64,227,206 RNU5A-7P, KICS2, 1 more genes
    nsv4767930insertion1nstd199human GRCh37 chr12: 64,597,803-64,597,803 , GRCh38.p12 chr12: 64,204,023-64,204,023 KICS2, RNU6-1009P
    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
    nsv4681587copy number variation1nstd102humanUncertain significance GRCh37 chr12: 64,173,731-64,895,171 , GRCh38.p12 chr12: 63,779,951-64,501,391 XPOT, LOC100420899, 16 more genes
    nsv4441621insertion1nstd175human GRCh37 chr12: 64,597,828-64,597,828 , GRCh38.p12 chr12: 64,204,048-64,204,048 KICS2, RNU6-1009P
    nsv4345788sequence alteration1nstd166human GRCh37.p13 chr12: 59,785,153-101,478,055 , GRCh38.p12 chr12: 59,391,372-101,084,277 , APAF1, 538 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
    nsv3933693insertion1nstd167human GRCh37 chr12: 64,597,828-64,597,828 , GRCh38.p12 chr12: 64,204,048-64,204,048 KICS2, RNU6-1009P
    nsv3916302copy number variation1nstd102humanPathogenic NCBI36 chr12: 59,587,199-65,248,124 , GRCh37 chr12: 61,300,932-66,961,857 , GRCh38 chr12: 60,907,151-66,568,077 LOC105369809, SRGAP1, 93 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 , BTG1P1, 2451 more genes
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