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Items: 1 to 20 of 249

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv5496786copy number variation1nstd206human GRCh38 chr12: 66,219,320-66,232,348 , GRCh37.p13 chr12: 66,613,100-66,626,128 RBMS1P1, IRAK3
    nsv5197493mobile element insertion1nstd203human GRCh38 chr12: 66,207,759-66,207,774 , GRCh37.p13 chr12: 66,601,539-66,601,554 IRAK3
    nsv5127068mobile element insertion1nstd203human GRCh38 chr12: 66,220,514-66,220,538 , GRCh37.p13 chr12: 66,614,294-66,614,318 IRAK3
    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
    nsv5008596copy number variation1nstd200human GRCh38 chr12: 66,212,822-66,213,230 , GRCh37.p13 chr12: 66,606,602-66,607,010 IRAK3
    nsv4995032copy number variation1nstd200human GRCh38 chr12: 66,226,337-66,227,754 , GRCh37.p13 chr12: 66,620,117-66,621,534 IRAK3
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4844983copy number variation1nstd200human GRCh37 chr12: 66,606,602-66,607,010 , GRCh38.p12 chr12: 66,212,822-66,213,230 IRAK3
    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
    nsv4668520copy number variation1nstd186human GRCh37 chr12: 66,609,223-66,609,834 , GRCh38.p12 chr12: 66,215,443-66,216,054 IRAK3
    nsv4617485copy number variation2nstd183human GRCh37 chr12: 66,609,223-66,609,834 , GRCh38.p12 chr12: 66,215,443-66,216,054 IRAK3
    nsv4603273copy number variation1nstd183human GRCh37 chr12: 66,597,695-66,603,149 , GRCh38.p12 chr12: 66,203,915-66,209,369 IRAK3
    nsv4575990mobile element insertion1nstd166human GRCh37.p13 chr12: 66,621,743-66,621,743 , GRCh38.p12 chr12: 66,227,963-66,227,963 IRAK3
    nsv4512004mobile element insertion1nstd166human GRCh37.p13 chr12: 66,648,077-66,648,077 , GRCh38.p12 chr12: 66,254,297-66,254,297 IRAK3
    nsv4508413mobile element insertion1nstd166human GRCh37.p13 chr12: 66,586,499-66,586,499 , GRCh38.p12 chr12: 66,192,719-66,192,719 IRAK3
    nsv4456227copy number variation1nstd102humanUncertain significance GRCh37 chr12: 66,285,627-66,718,973 , GRCh38.p12 chr12: 65,891,847-66,325,193 HELB, LINC02425, 12 more genes
    nsv4368154copy number variation1nstd173human GRCh37 chr12: 66,506,631-66,806,420 , GRCh38.p12 chr12: 66,112,851-66,412,640 GRIP1, MIR6502, 9 more genes
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