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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7059031inversion1nstd229human GRCh38 chr15: 70,160,153-73,809,878 , GRCh37.p13 chr15: 70,452,492-74,102,219 CD276, LOC107984716, 71 more genes
    nsv6970675copy number variation1nstd229human GRCh38 chr15: 70,504,471-70,657,149 , GRCh37.p13 chr15: 70,796,810-70,949,488 LINC02204, UACA, 5 more genes
    nsv6967732copy number variation1nstd229human GRCh38 chr15: 70,606,085-70,614,895 , GRCh37.p13 chr15: 70,898,424-70,907,234 SALRNA3
    nsv6961707copy number variation1nstd229human GRCh38 chr15: 70,585,628-70,617,903 , GRCh37.p13 chr15: 70,877,967-70,910,242 LINC02204, SALRNA3
    nsv6637906copy number variation1nstd102humanUncertain significance GRCh37 chr15: 68,807,665-70,981,473 , GRCh38.p12 chr15: 68,515,326-70,689,134 UACA, RPLP1, 36 more genes
    nsv6637504copy number variation1nstd102humanUncertain significance GRCh37 chr15: 70,814,037-71,028,303 , GRCh38.p12 chr15: 70,521,698-70,735,964 SALRNA2, LINC02204, 4 more genes
    nsv6510424copy number variation1nstd223human GRCh38 chr15: 70,606,085-70,614,891 , GRCh37.p13 chr15: 70,898,424-70,907,230 SALRNA3
    nsv6504179copy number variation1nstd223human GRCh38 chr15: 70,615,833-70,616,501 , GRCh37.p13 chr15: 70,908,172-70,908,840 SALRNA3
    nsv6132964copy number variation1nstd213human GRCh37 chr15: 70,890,000-71,180,001 , GRCh38.p12 chr15: 70,597,661-70,887,662 LRRC49, UACA, 7 more genes
    nsv6132961copy number variation1nstd213human GRCh37 chr15: 69,080,000-73,430,001 , GRCh38.p12 chr15: 68,787,661-73,137,660 BBS4, MYO9A, 84 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv4728893copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 70,268,937-74,098,081 , GRCh38.p12 chr15: 69,976,598-73,805,740 BBS4, FKBP1AP2, 75 more genes
    nsv4704343copy number variation1nstd195human GRCh37 chr15: 70,665,951-70,911,901 , GRCh38.p12 chr15: 70,373,612-70,619,562 LINC02204, SALRNA3, 2 more genes
    nsv4678891copy number variation1nstd189human GRCh37.p13 chr15: 70,843,178-71,191,788 , GRCh38.p12 chr15: 70,550,839-70,899,449 LRRC49, UACA, 9 more genes
    nsv4338323sequence alteration1nstd166human GRCh37.p13 chr15: 69,446,476-72,211,091 , GRCh38.p12 chr15: 69,154,137-71,918,750 , MYO9A, 45 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3920633copy number variation1nstd102humanPathogenic GRCh38 chr15: 68,830,574-73,823,337 , NCBI36 chr15: 66,909,967-71,902,731 , GRCh37 chr15: 69,122,913-74,115,678 NEO1, LOC390600, 95 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
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