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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142664copy number variation1nstd232human GRCh37.p13 chr12: 95,542,937-95,542,995 , GRCh38.p12 chr12: 95,149,161-95,149,219 FGD6
    nsv7076772inversion1nstd229human GRCh38 chr12: 95,104,156-95,107,172 , GRCh37.p13 chr12: 95,497,932-95,500,948 FGD6
    nsv7065284inversion1nstd229human GRCh38 chr12: 94,129,761-97,319,471 , GRCh37.p13 chr12: 94,523,537-97,713,249 AMDHD1, TMCC3, 62 more genes
    nsv6936824copy number variation1nstd229human GRCh38 chr12: 95,102,340-95,113,010 , GRCh37.p13 chr12: 95,496,116-95,506,786 FGD6
    nsv6936248copy number variation1nstd229human GRCh38 chr12: 95,204,011-95,207,279 , GRCh37.p13 chr12: 95,597,787-95,601,055 FGD6
    nsv6934787copy number variation1nstd229human GRCh38 chr12: 95,158,574-95,158,748 , GRCh37.p13 chr12: 95,552,350-95,552,524 FGD6
    nsv6933641copy number variation1nstd229human GRCh38 chr12: 95,192,824-95,196,290 , GRCh37.p13 chr12: 95,586,600-95,590,066 FGD6
    nsv6929747copy number variation1nstd229human GRCh38 chr12: 95,126,601-95,271,900 , GRCh37.p13 chr12: 95,520,377-95,665,676 FGD6, VEZT, 1 more genes
    nsv6929244copy number variation1nstd229human GRCh38 chr12: 95,164,201-95,172,300 , GRCh37.p13 chr12: 95,557,977-95,566,076 FGD6
    nsv6929146copy number variation1nstd229human GRCh38 chr12: 95,026,960-95,492,756 , GRCh37.p13 chr12: 95,420,736-95,886,532 LOC107984545, LOC100287148, 12 more genes
    nsv6928576copy number variation1nstd229human GRCh38 chr12: 95,085,722-95,087,508 , GRCh37.p13 chr12: 95,479,498-95,481,284 FGD6
    nsv6928459copy number variation1nstd229human GRCh38 chr12: 95,165,136-95,211,187 , GRCh37.p13 chr12: 95,558,912-95,604,963 FGD6
    nsv6927838copy number variation1nstd229human GRCh38 chr12: 95,076,397-95,076,429 , GRCh37.p13 chr12: 95,470,173-95,470,205 FGD6
    nsv6927794copy number variation1nstd229human GRCh38 chr12: 94,895,518-95,127,063 , GRCh37.p13 chr12: 95,289,294-95,520,839 NDUFA12, LOC105369915, 4 more genes
    nsv6926652copy number variation1nstd229human GRCh38 chr12: 95,123,066-95,174,949 , GRCh37.p13 chr12: 95,516,842-95,568,725 FGD6, RPL14P4
    nsv6926063copy number variation1nstd229human GRCh38 chr12: 95,125,985-95,196,270 , GRCh37.p13 chr12: 95,519,761-95,590,046 FGD6, RPL14P4
    nsv6925845copy number variation1nstd229human GRCh38 chr12: 95,120,668-95,126,789 , GRCh37.p13 chr12: 95,514,444-95,520,565 FGD6, RPL14P4
    nsv6924567copy number variation1nstd229human GRCh38 chr12: 95,117,790-95,121,187 , GRCh37.p13 chr12: 95,511,566-95,514,963 FGD6
    nsv6922475copy number variation1nstd229human GRCh38 chr12: 95,192,242-95,199,887 , GRCh37.p13 chr12: 95,586,018-95,593,663 FGD6
    nsv6921571copy number variation1nstd229human GRCh38 chr12: 95,172,482-95,182,397 , GRCh37.p13 chr12: 95,566,258-95,576,173 FGD6
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