U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 190

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5886288copy number variation1nstd209human GRCh38 chr1: 11,029,849-11,029,913 , GRCh37.p13 chr1: 11,089,906-11,089,970 TARDBP, MASP2
    nsv5876575copy number variation1nstd209human GRCh38 chr1: 11,010,704-11,011,411 , GRCh37.p13 chr1: 11,070,761-11,071,468 TARDBP
    nsv5557473sequence alteration1nstd206human GRCh38 chr1: 10,919,048-11,710,696 , GRCh37.p13 chr1: 10,979,105-11,770,753 , ANGPTL7, 26 more genes
    nsv5420963copy number variation1nstd206human GRCh38 chr1: 11,021,429-11,021,526 , GRCh37.p13 chr1: 11,081,486-11,081,583 TARDBP
    nsv5418343copy number variation1nstd206human GRCh38 chr1: 11,010,704-11,011,445 , GRCh37.p13 chr1: 11,070,761-11,071,502 TARDBP
    nsv5363886translocation1nstd200human GRCh38 chr1: 11,022,369-11,022,369 , GRCh38 chr1: 11,023,357-11,023,357 , GRCh37.p13 chr1: 11,082,426-11,082,426 , GRCh37.p13 chr1: 11,083,414-11,083,414 TARDBP
    nsv5344053translocation1nstd200human GRCh37 chr1: 11,083,414-11,083,414 , GRCh37 chr1: 11,082,426-11,082,426 , GRCh38.p12 chr1: 11,023,357-11,023,357 , GRCh38.p12 chr1: 11,022,369-11,022,369 TARDBP
    nsv5286679copy number variation1nstd204human GRCh38.p13 chr1: 11,014,899-11,015,563 , GRCh37.p13 chr1: 11,074,956-11,075,620 TARDBP
    nsv5190248mobile element insertion1nstd203human GRCh38 chr1: 11,017,653-11,017,668 , GRCh37.p13 chr1: 11,077,710-11,077,725 TARDBP
    nsv5066364mobile element insertion1nstd203human GRCh38 chr1: 11,017,653-11,017,668 , GRCh37.p13 chr1: 11,077,710-11,077,725 TARDBP
    nsv4903062copy number variation1nstd200human GRCh38 chr1: 11,024,648-11,030,862 , GRCh37.p13 chr1: 11,084,705-11,090,919 MASP2, TARDBP
    nsv4782956copy number variation1nstd200human GRCh37 chr1: 11,074,965-11,075,613 , GRCh38.p12 chr1: 11,014,908-11,015,556 TARDBP
    nsv4782954copy number variation1nstd200human GRCh37 chr1: 11,068,899-11,070,919 , GRCh38.p12 chr1: 11,008,842-11,010,862 TARDBP
    nsv4772162copy number variation1nstd200human GRCh37 chr1: 11,084,705-11,090,920 , GRCh38.p12 chr1: 11,024,648-11,030,863 MASP2, TARDBP
    nsv4684113copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 11,053,101-11,336,968 , GRCh38.p12 chr1: 10,993,044-11,276,911 MTOR, EXOSC10, 11 more genes
    nsv4681090copy number variation1nstd102humanUncertain significance GRCh37 chr1: 11,072,691-11,994,922 , GRCh38.p12 chr1: 11,012,634-11,934,865 FBXO44, LINC01647, 36 more genes
    nsv4674729copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,908,411-11,158,092 , GRCh38.p12 chr1: 10,848,354-11,098,035 CFL1P6, SRM, 7 more genes
    nsv4674113copy number variation1nstd102humanUncertain significance GRCh37 chr1: 11,086,990-11,429,365 , GRCh38.p12 chr1: 11,026,933-11,369,308 RNU6-537P, UBE2V2P3, 13 more genes
    nsv4674003copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 9,852,396-11,909,475 , GRCh38.p12 chr1: 9,792,338-11,849,418 CLCN6, CORT, 59 more genes
    nsv4579015copy number variation1nstd183human GRCh37 chr1: 11,085,842-11,090,892 , GRCh38.p12 chr1: 11,025,785-11,030,835 TARDBP, MASP2
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center
    -