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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923742copy number variation1nstd209human GRCh38 chr12: 21,398,810-28,763,815 , GRCh37.p13 chr12: 21,551,744-28,916,748 , LOC105369710, 101 more genes
    nsv5916901copy number variation1nstd209human GRCh38 chr12: 21,398,719-28,763,765 , GRCh37.p13 chr12: 21,551,653-28,916,698 , LOC105369704, 101 more genes
    nsv5497910copy number variation1nstd206human GRCh38 chr12: 25,198,038-25,205,984 , GRCh37.p13 chr12: 25,350,972-25,358,918 ETFRF1, KRAS
    nsv5379601translocation1nstd200human GRCh38 chr12: 25,208,370-25,208,370 , GRCh38 chr19: 20,696,863-20,696,863 , GRCh37.p13 chr12: 25,361,304-25,361,304 , GRCh37.p13 chr19: 20,879,669-20,879,669 LOC100533638, KRAS
    nsv5355637translocation1nstd200human GRCh38 chr19: 20,696,848-20,696,848 , GRCh38 chr12: 25,250,920-25,250,920 , GRCh37.p13 chr12: 25,403,854-25,403,854 , GRCh37.p13 chr19: 20,879,654-20,879,654 KRAS, LOC100533638
    nsv5355636translocation1nstd200human GRCh38 chr12: 25,225,612-25,225,612 , GRCh38 chr12: 25,209,914-25,209,914 , GRCh37.p13 chr12: 25,362,848-25,362,848 , GRCh37.p13 chr12: 25,378,546-25,378,546 KRAS
    nsv5345461translocation1nstd200human GRCh37 chr12: 25,399,864-25,399,864 , GRCh37 chr12: 25,399,931-25,399,931 , GRCh38.p12 chr12: 25,246,930-25,246,930 , GRCh38.p12 chr12: 25,246,997-25,246,997 KRAS
    nsv4981623copy number variation1nstd200human GRCh38 chr12: 25,246,930-25,246,997 , GRCh37.p13 chr12: 25,399,864-25,399,931 KRAS
    nsv4981622copy number variation1nstd200human GRCh38 chr12: 25,215,277-25,219,947 , GRCh37.p13 chr12: 25,368,211-25,372,881 KRAS
    nsv4981621copy number variation1nstd200human GRCh38 chr12: 25,214,470-25,216,537 , GRCh37.p13 chr12: 25,367,404-25,369,471 KRAS
    nsv4974448copy number variation1nstd200human GRCh38 chr12: 24,581,434-25,314,724 , GRCh37.p13 chr12: 24,734,368-25,467,658 , LOC105369699, 15 more genes
    nsv4974447copy number variation1nstd200human GRCh38 chr12: 24,537,362-25,205,348 , GRCh37.p13 chr12: 24,690,296-25,358,282 , DAD1P1, 16 more genes
    nsv4706811copy number variation1nstd195human GRCh38.p12 chr12: 25,174,967-25,482,517 , GRCh37 chr12: 25,327,901-25,635,451 KRAS, DNAI7, 7 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4527766copy number variation1nstd166human GRCh37.p13 chr12: 25,377,810-25,378,252 , GRCh38.p12 chr12: 25,224,876-25,225,318 KRAS
    nsv4504627mobile element insertion1nstd166human GRCh37.p13 chr12: 25,362,302-25,362,302 , GRCh38.p12 chr12: 25,209,368-25,209,368 KRAS
    nsv4456793copy number variation1nstd102humanPathogenic GRCh37 chr12: 16,141,429-27,733,325 , GRCh38.p12 chr12: 15,988,495-27,580,392 PDE3A, ETFRF1, 133 more genes
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
    nsv4454594copy number variation1nstd102humanUncertain significance GRCh37 chr12: 25,362,709-25,398,338 , GRCh38 chr12: 25,209,775-25,245,404 KRAS
    nsv4454590copy number variation1nstd102humanUncertain significance GRCh38 chr12: 25,209,775-25,209,931 , GRCh37 chr12: 25,362,709-25,362,865 KRAS
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