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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977237insertion1nstd209human GRCh38 chr12: 10,293,157-10,293,157 , GRCh37.p13 chr12: 10,445,756-10,445,756 KLRD1
    nsv5976275inversion1nstd209human GRCh38 chr12: 10,296,446-11,054,973 , GRCh37.p13 chr12: 10,449,045-11,207,572 , KLRC1, 40 more genes
    nsv5921512copy number variation1nstd209human GRCh38 chr12: 10,254,813-10,255,121 , GRCh37.p13 chr12: 10,407,412-10,407,720 KLRD1
    nsv5705147mobile element insertion2nstd211human GRCh38 chr12: 10,262,815-10,262,815 , GRCh37.p13 chr12: 10,415,414-10,415,414 KLRD1
    nsv5660125insertion1nstd207human GRCh38 chr12: 10,293,157-10,293,157 , GRCh37.p13 chr12: 10,445,756-10,445,756 KLRD1
    nsv5659579insertion1nstd207human GRCh38 chr12: 10,250,243-10,250,243 , GRCh37.p13 chr12: 10,402,842-10,402,842 KLRD1
    nsv5655000insertion1nstd207human GRCh38 chr12: 10,293,161-10,293,161 , GRCh37.p13 chr12: 10,445,760-10,445,760 KLRD1
    nsv5647890insertion1nstd207human GRCh38 chr12: 10,262,802-10,262,802 , GRCh37.p13 chr12: 10,415,401-10,415,401 KLRD1
    nsv5597208copy number variation1nstd207human GRCh38 chr12: 10,254,813-10,255,121 , GRCh37.p13 chr12: 10,407,412-10,407,720 KLRD1
    nsv5592574copy number variation1nstd207human GRCh38 chr12: 10,240,379-10,258,107 , GRCh37.p13 chr12: 10,392,978-10,410,706 KLRD1
    nsv5513590copy number variation1nstd206human GRCh38 chr12: 10,256,771-10,256,854 , GRCh37.p13 chr12: 10,409,370-10,409,453 KLRD1
    nsv5513115copy number variation1nstd206human GRCh38 chr12: 10,263,536-10,263,837 , GRCh37.p13 chr12: 10,416,135-10,416,436 KLRD1
    nsv5509199copy number variation1nstd206human GRCh38 chr12: 10,254,813-10,255,122 , GRCh37.p13 chr12: 10,407,412-10,407,721 KLRD1
    nsv5502925copy number variation1nstd206human GRCh38 chr12: 10,248,595-10,250,512 , GRCh37.p13 chr12: 10,401,194-10,403,111 KLRD1
    nsv5499264copy number variation1nstd206human GRCh38 chr12: 10,240,383-10,258,108 , GRCh37.p13 chr12: 10,392,982-10,410,707 KLRD1
    nsv5416821mobile element insertion1nstd206human GRCh38 chr12: 10,262,815-10,262,866 , GRCh37.p13 chr12: 10,415,414-10,415,465 KLRD1
    nsv5392169copy number variation3nstd186human GRCh37 chr12: 10,407,412-10,407,721 , GRCh38.p12 chr12: 10,254,813-10,255,122 KLRD1
    nsv5348580translocation1nstd200human GRCh38 chr12: 10,258,108-10,258,108 , GRCh38 chr12: 10,240,383-10,240,383 , GRCh37.p13 chr12: 10,392,982-10,392,982 , GRCh37.p13 chr12: 10,410,707-10,410,707 KLRD1
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5309910copy number variation1nstd204human GRCh38.p13 chr12: 10,240,360-10,258,137 , GRCh37.p13 chr12: 10,392,959-10,410,736 KLRD1
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