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 248

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094183copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083 LOC112268078, LRTOMT, 142 more genes
    nsv6916207copy number variation1nstd229human GRCh38 chr11: 71,861,769-71,865,034 , GRCh37.p13 chr11: 71,572,815-71,576,080 DEFB130C, XNDC1N
    nsv6913971copy number variation1nstd229human GRCh38 chr11: 71,900,488-71,900,560 , GRCh37.p13 chr11: 71,611,534-71,611,606 XNDC1N
    nsv6913264copy number variation1nstd229human GRCh38 chr11: 71,864,487-71,880,600 , GRCh37.p13 chr11: 71,575,533-71,591,646 XNDC1N, DEFB131B
    nsv6911485copy number variation1nstd229human GRCh38 chr11: 71,919,659-71,925,737 , GRCh37.p13 chr11: 71,630,705-71,636,783 XNDC1N
    nsv6910311copy number variation1nstd229human GRCh38 chr11: 71,721,399-71,910,691 , GRCh37.p13 chr11: 71,432,445-71,621,737 RNA5SP342, FAM86C1P, 9 more genes
    nsv6909541copy number variation1nstd229human GRCh38 chr11: 71,924,444-71,927,300 , GRCh37.p13 chr11: 71,635,490-71,638,346 RNF121, XNDC1N
    nsv6908275copy number variation1nstd229human GRCh38 chr11: 71,281,500-72,194,614 , GRCh37.p13 chr11: 71,088,949-71,905,658 DEFB130C, ANAPC15, 40 more genes
    nsv6906184copy number variation1nstd229human GRCh38 chr11: 71,914,622-71,917,990 , GRCh37.p13 chr11: 71,625,668-71,629,036 XNDC1N
    nsv6901393copy number variation1nstd229human GRCh38 chr11: 71,893,001-71,903,300 , GRCh37.p13 chr11: 71,604,047-71,614,346 OR7E128P, XNDC1N, 1 more genes
    nsv6899851copy number variation1nstd229human GRCh38 chr11: 71,885,111-71,885,187 , GRCh37.p13 chr11: 71,596,157-71,596,233 XNDC1N
    nsv6637237copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,051,703-71,655,505 , GRCh38.p12 chr11: 71,340,657-71,944,459 FAM86C1P, KRTAP5-7, 28 more genes
    nsv6589036inversion1nstd223human GRCh38 chr11: 71,922,033-71,922,424 , GRCh37.p13 chr11: 71,633,079-71,633,470 XNDC1N
    nsv6473099copy number variation1nstd223human GRCh38 chr11: 71,861,279-71,864,272 , GRCh37.p13 chr11: 71,572,325-71,575,318 XNDC1N, DEFB130C
    nsv6472608copy number variation1nstd223human GRCh38 chr11: 71,884,901-71,886,800 , GRCh37.p13 chr11: 71,595,947-71,597,846 XNDC1N, DEFB131B
    nsv6472495copy number variation1nstd223human GRCh38 chr11: 71,600,178-71,900,170 , GRCh37.p13 chr11: 71,311,224-71,611,216 DEFB130C, ENPP7P8, 13 more genes
    nsv6471674copy number variation1nstd223human GRCh38 chr11: 71,890,677-71,892,041 , GRCh37.p13 chr11: 71,601,723-71,603,087 OR7E128P, XNDC1N
    nsv6471204copy number variation1nstd223human GRCh38 chr11: 71,909,917-71,910,868 , GRCh37.p13 chr11: 71,620,963-71,621,914 XNDC1N
    nsv6468796copy number variation1nstd223human GRCh38 chr11: 71,890,762-71,912,769 , GRCh37.p13 chr11: 71,601,808-71,623,815 OR7E126P, XNDC1N, 1 more genes
    nsv6462604copy number variation1nstd223human GRCh38 chr11: 71,587,217-71,887,226 , GRCh37.p13 chr11: 71,298,263-71,598,272 RPS3AP41, XNDC1N, 13 more genes
    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