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 151

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099241copy number variation1nstd231human GRCh38.p12 chr1: 161,703,753-165,575,316 , GRCh37 chr1: 161,673,543-165,544,553 LMX1A, DDR2, 49 more genes
    nsv7095487copy number variation1nstd102humanUncertain significance GRCh37 chr1: 161,279,609-161,751,809 , GRCh38.p12 chr1: 161,309,819-161,782,019 FCGR2C, RNU6-481P, 56 more genes
    nsv7057537inversion1nstd229human GRCh38 chr1: 161,493,525-166,518,262 , GRCh37.p13 chr1: 161,463,315-166,487,499 LOC107985451, ALDH9A1, 88 more genes
    nsv7042802inversion1nstd229human GRCh38 chr1: 159,324,839-163,640,188 , GRCh37.p13 chr1: 159,294,629-163,609,919 TRG-GCC2-1, LOC107985220, 178 more genes
    nsv7039884inversion1nstd229human GRCh38 chr1: 159,817,036-167,858,499 , GRCh37.p13 chr1: 159,786,826-167,827,737 TRP-AGG2-1, FCGR2C, 228 more genes
    nsv6643165copy number variation1nstd229human GRCh38 chr1: 161,751,301-161,759,400 , GRCh37.p13 chr1: 161,721,091-161,729,190 DUSP12
    nsv6332269copy number variation1nstd223human GRCh38 chr1: 160,388,767-162,811,116 , GRCh37.p13 chr1: 160,358,557-162,780,906 ATF6-DT, RPS23P10, 119 more genes
    nsv6313604copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,417,296-166,197,042 , GRCh38.p12 chr1: 160,447,506-166,227,805 USF1, TRE-CTC1-3, 161 more genes
    nsv6310598copy number variation1nstd102humanUncertain significance GRCh37 chr1: 161,645,027-161,772,082 , GRCh38.p12 chr1: 161,675,237-161,802,292 FCGR2B, FCRLB, 6 more genes
    nsv6310595copy number variation2nstd102humanUncertain significance GRCh37 chr1: 158,581,054-162,750,036 , GRCh38.p12 chr1: 158,611,264-162,780,246 IGSF8, SETP9, 193 more genes
    nsv6223833insertion1nstd214human GRCh38 chr1: 161,753,756-161,753,756 , GRCh37.p13 chr1: 161,723,546-161,723,546 DUSP12
    nsv6133934copy number variation1nstd213human GRCh37 chr1: 161,630,000-164,240,001 , GRCh38.p12 chr1: 161,660,210-164,270,764 FCGR2B, NOS1AP, 35 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133590copy number variation1nstd213human GRCh37 chr1: 161,630,000-161,880,001 , GRCh38.p12 chr1: 161,660,210-161,910,211 FCGR2B, DUSP12, 7 more genes
    nsv6117825copy number variation1nstd186human GRCh37 chr1: 161,723,546-161,723,605 , GRCh38.p12 chr1: 161,753,756-161,753,815 DUSP12
    nsv5969343inversion1nstd209human GRCh38 chr1: 161,566,673-161,918,703 , GRCh37.p13 chr1: 161,536,463-161,888,493 FCGR2B, FCGR3B, 12 more genes
    nsv5881058copy number variation1nstd209human GRCh38 chr1: 161,697,901-161,830,547 , GRCh37.p13 chr1: 161,667,691-161,800,337 DUSP12, ATF6, 4 more genes
    nsv5620363insertion1nstd207human GRCh38 chr1: 161,753,756-161,753,756 , GRCh37.p13 chr1: 161,723,546-161,723,546 DUSP12
    nsv5606011insertion1nstd207human GRCh38 chr1: 161,750,900-161,750,900 , GRCh37.p13 chr1: 161,720,690-161,720,690 DUSP12
    nsv5425338copy number variation1nstd206human GRCh38 chr1: 161,753,756-161,753,815 , GRCh37.p13 chr1: 161,723,546-161,723,605 DUSP12
    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