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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5710511mobile element insertion1nstd211human GRCh38 chr12: 9,839,404-9,839,404 , GRCh37.p13 chr12: 9,992,000-9,992,000 KLRF1
    nsv5504954copy number variation1nstd206human GRCh38 chr12: 9,819,640-9,825,440 , GRCh37.p13 chr12: 9,972,236-9,978,036 KLRF1
    nsv5496951copy number variation1nstd206human GRCh38 chr12: 9,803,957-9,809,772 , GRCh37.p13 chr12: 9,956,553-9,962,368 KLRF1
    nsv5425825mobile element insertion1nstd206human GRCh38 chr12: 9,839,404-9,839,446 , GRCh37.p13 chr12: 9,992,000-9,992,042 KLRF1
    nsv5348574translocation1nstd200human GRCh38 chr12: 9,809,772-9,809,772 , GRCh38 chr12: 9,803,957-9,803,957 , GRCh37.p13 chr12: 9,962,368-9,962,368 , GRCh37.p13 chr12: 9,956,553-9,956,553 KLRF1
    nsv5340982translocation1nstd200human GRCh37 chr12: 9,956,553-9,956,553 , GRCh37 chr12: 9,962,368-9,962,368 , GRCh38.p12 chr12: 9,803,957-9,803,957 , GRCh38.p12 chr12: 9,809,772-9,809,772 KLRF1
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5184036mobile element insertion1nstd203human GRCh38 chr12: 9,820,058-9,820,074 , GRCh37.p13 chr12: 9,972,654-9,972,670 KLRF1
    nsv5135013mobile element insertion1nstd203human GRCh38 chr12: 9,841,990-9,842,004 , GRCh37.p13 chr12: 9,994,589-9,994,603 KLRF1
    nsv5134867mobile element insertion1nstd203human GRCh38 chr12: 9,839,387-9,839,404 , GRCh37.p13 chr12: 9,991,983-9,992,000 KLRF1
    nsv5130930mobile element insertion1nstd203human GRCh38 chr12: 9,805,685-9,805,696 , GRCh37.p13 chr12: 9,958,281-9,958,292 KLRF1
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4846699copy number variation1nstd200human GRCh37 chr12: 9,939,260-9,961,462 , GRCh38.p12 chr12: 9,786,664-9,808,866 KLRF1
    nsv4841163copy number variation1nstd200human GRCh37 chr12: 9,972,236-9,978,036 , GRCh38.p12 chr12: 9,819,640-9,825,440 KLRF1
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4664094copy number variation1nstd186human GRCh37 chr12: 9,915,398-10,038,593 , GRCh38.p12 chr12: 9,762,802-9,885,994 CLEC2B, KLRF1, 3 more genes
    nsv4657591copy number variation1nstd186human GRCh37 chr12: 9,915,398-10,038,593 , GRCh38.p12 chr12: 9,762,802-9,885,994 CLEC2B, KLRF1, 3 more genes
    nsv4612688copy number variation1nstd183human GRCh37 chr12: 9,820,575-10,014,304 , GRCh38.p12 chr12: 9,667,979-9,861,705 CD69, CLEC2B, 6 more genes
    nsv4511746mobile element insertion1nstd166human GRCh37.p13 chr12: 9,958,281-9,958,281 , GRCh38.p12 chr12: 9,805,685-9,805,685 KLRF1
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