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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947241copy number variation1nstd209human GRCh38 chr12: 59,520,307-59,523,007 , GRCh37.p13 chr12: 59,914,088-59,916,788 LINC02448
    nsv5494149copy number variation1nstd206human GRCh38 chr12: 59,262,369-59,610,125 , GRCh37.p13 chr12: 59,656,150-60,003,906 RNU6-279P, RNU6-871P, 3 more genes
    nsv5121206mobile element insertion1nstd203human GRCh38 chr12: 59,522,295-59,522,311 , GRCh37.p13 chr12: 59,916,076-59,916,092 LINC02448
    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
    nsv4985671copy number variation1nstd200human GRCh38 chr12: 59,262,369-59,610,125 , GRCh37.p13 chr12: 59,656,150-60,003,906 RNU6-871P, RNU6-279P, 3 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    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
    nsv4728909copy number variation1nstd102humanUncertain significance GRCh37 chr12: 59,136,522-62,410,625 , GRCh38.p12 chr12: 58,742,740-62,016,844 KRT8P19, METTL15P2, 17 more genes
    nsv4675978copy number variation1nstd102humanUncertain significance GRCh37 chr12: 59,659,908-60,004,443 , GRCh38.p12 chr12: 59,266,127-59,610,662 SLC16A7, RNU6-871P, 3 more genes
    nsv4675143copy number variation1nstd102humanPathogenic GRCh37 chr12: 55,552,371-62,126,304 , GRCh38.p12 chr12: 55,158,587-61,732,523 OR6C71P, METTL1, 183 more genes
    nsv4416260copy number variation1nstd174human GRCh37 chr12: 59,659,871-60,004,241 , GRCh38.p12 chr12: 59,266,090-59,610,460 LINC02448, SLC16A7, 3 more genes
    nsv4375587copy number variation1nstd173human GRCh37 chr12: 59,374,630-59,983,402 , GRCh38.p12 chr12: 58,980,849-59,589,621 LINC02448, LRIG3-DT, 5 more genes
    nsv4370952copy number variation1nstd173human GRCh37 chr12: 59,138,864-60,247,169 , GRCh38.p12 chr12: 58,745,082-59,853,388 SLC16A7, LRIG3-DT, 10 more genes
    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
    nsv4206920copy number variation1nstd166human GRCh37.p13 chr12: 59,839,656-60,973,143 , GRCh38.p12 chr12: 59,445,875-60,579,362 SLC16A7, LOC100996696, 4 more genes
    nsv4194682copy number variation1nstd166human GRCh37.p13 chr12: 59,656,122-60,003,933 , GRCh38.p12 chr12: 59,262,341-59,610,152 RNU6-871P, SLC16A7, 3 more genes
    nsv3966754copy number variation1nstd168human GRCh38 chr12: 59,497,392-59,576,745 , GRCh37.p13 chr12: 59,891,173-59,970,526 LINC02448
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