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Items: 1 to 20 of 263

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970675insertion1nstd209human GRCh38 chr11: 111,981,071-111,981,071 , GRCh37.p13 chr11: 111,851,796-111,851,796 , GRCh37.p13 chr11|NW_003871080.1: 233,062-233,062 DIXDC1
    nsv5920873copy number variation1nstd209human GRCh38 chr11: 111,950,351-111,950,488 , GRCh37.p13 chr11: 111,821,075-111,821,212 , GRCh37.p13 chr11|NW_003871080.1: 202,342-202,479 DIXDC1
    nsv5711783mobile element insertion2nstd211human GRCh38 chr11: 111,981,087-111,981,087 , GRCh37.p13 chr11|NW_003871080.1: 233,078-233,078 , GRCh37.p13 chr11: 111,851,812-111,851,812 DIXDC1
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5650110insertion1nstd207human GRCh38 chr11: 111,981,071-111,981,071 , GRCh37.p13 chr11|NW_003871080.1: 233,062-233,062 , GRCh37.p13 chr11: 111,851,796-111,851,796 DIXDC1
    nsv5512386copy number variation1nstd206human GRCh38 chr11: 111,959,468-111,959,596 , GRCh37.p13 chr11: 111,830,192-111,830,320 , GRCh37.p13 chr11|NW_003871080.1: 211,459-211,587 DIXDC1
    nsv5511033copy number variation1nstd206human GRCh38 chr11: 112,021,428-112,021,501 , GRCh37.p13 chr11: 111,892,152-111,892,225 , GRCh37.p13 chr11|NW_003871080.1: 273,419-273,492 DIXDC1
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5505796copy number variation1nstd206human GRCh38 chr11: 112,022,549-112,024,925 , GRCh37.p13 chr11|NW_003871080.1: 274,540-276,916 , GRCh37.p13 chr11: 111,893,273-111,895,649 DLAT, DIXDC1
    nsv5505732copy number variation1nstd206human GRCh38 chr11: 111,947,121-111,954,445 , GRCh37.p13 chr11|NW_003871080.1: 199,112-206,436 , GRCh37.p13 chr11: 111,817,845-111,825,169 DIXDC1
    nsv5505030copy number variation1nstd206human GRCh38 chr11: 112,006,197-112,006,254 , GRCh37.p13 chr11|NW_003871080.1: 258,188-258,245 , GRCh37.p13 chr11: 111,876,921-111,876,978 DIXDC1
    nsv5504634copy number variation1nstd206human GRCh38 chr11: 111,957,740-111,958,199 , GRCh37.p13 chr11|NW_003871080.1: 209,731-210,190 , GRCh37.p13 chr11: 111,828,464-111,828,923 DIXDC1
    nsv5431372mobile element insertion1nstd206human GRCh38 chr11: 111,981,087-111,981,138 , GRCh37.p13 chr11|NW_003871080.1: 233,078-233,129 , GRCh37.p13 chr11: 111,851,812-111,851,863 DIXDC1
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5301544copy number variation1nstd204human GRCh38.p13 chr11: 111,954,072-111,968,025 , GRCh37.p13 chr11|NW_003871080.1: 206,063-220,016 , GRCh37.p13 chr11: 111,824,796-111,838,749 DIXDC1
    nsv5276629copy number variation1nstd204human GRCh38.p13 chr11: 111,954,301-111,967,542 , GRCh37.p13 chr11|NW_003871080.1: 206,292-219,533 , GRCh37.p13 chr11: 111,825,025-111,838,266 DIXDC1
    nsv5189663mobile element insertion1nstd203human GRCh38 chr11: 111,995,946-111,995,957 , GRCh37.p13 chr11|NW_003871080.1: 247,937-247,948 , GRCh37.p13 chr11: 111,866,670-111,866,681 DIXDC1
    nsv5136648mobile element insertion1nstd203human GRCh38 chr11: 112,007,817-112,007,825 , GRCh37.p13 chr11: 111,878,541-111,878,549 , GRCh37.p13 chr11|NW_003871080.1: 259,808-259,816 DIXDC1
    nsv5136434mobile element insertion1nstd203human GRCh38 chr11: 111,981,076-111,981,087 , GRCh37.p13 chr11|NW_003871080.1: 233,067-233,078 , GRCh37.p13 chr11: 111,851,801-111,851,812 DIXDC1
    nsv5135696mobile element insertion1nstd203human GRCh38 chr11: 111,966,397-111,966,402 , GRCh37.p13 chr11|NW_003871080.1: 218,388-218,393 , GRCh37.p13 chr11: 111,837,121-111,837,126 DIXDC1
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