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 154

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7065616inversion1nstd229human GRCh38 chr11: 55,877,934-56,853,091 , GRCh37.p13 chr11: 55,645,410-56,620,567 OR5M5P, OR5G3, 74 more genes
    nsv7064532inversion1nstd229human GRCh38 chr11: 55,878,162-56,072,221 , GRCh37.p13 chr11: 55,645,638-55,839,697 OR7E5P, OR5I1, 12 more genes
    nsv6915715copy number variation1nstd229human GRCh38 chr11: 55,847,722-55,933,858 , GRCh37.p13 chr11: 55,615,198-55,701,334 OR5I1, TRIM51, 5 more genes
    nsv6905659copy number variation1nstd229human GRCh38 chr11: 55,882,088-55,896,820 , GRCh37.p13 chr11: 55,649,564-55,664,296 TRIM51
    nsv6903817copy number variation1nstd229human GRCh38 chr11: 55,889,039-57,077,059 , GRCh37.p13 chr11: 55,656,515-56,844,534 OR5J1P, OR8H1, 83 more genes
    nsv6621250copy number variation1nstd224human GRCh37 chr11: 55,595,455-55,690,371 , GRCh38.p12 chr11: 55,827,979-55,922,895 OR5L2, OR9M1P, 6 more genes
    nsv6621249copy number variation1nstd224human GRCh37 chr11: 55,171,027-56,905,911 , GRCh38.p12 chr11: 55,403,551-57,138,437 OR5I1, OR8K2P, 113 more genes
    nsv6621189copy number variation1nstd224human GRCh37 chr11: 55,659,089-55,762,038 , GRCh38.p12 chr11: 55,891,613-55,994,562 OR5I1, OR5W1P, 7 more genes
    nsv6621186copy number variation2nstd224human GRCh37 chr11: 54,794,237-56,003,589 , GRCh38.p12 chr11: 55,026,761-56,236,113 OR5L2, OR9M1P, 65 more genes
    nsv6621001copy number variation2nstd224human GRCh37 chr11: 55,594,936-55,690,371 , GRCh38.p12 chr11: 55,827,460-55,922,895 OR5L2, OR9M1P, 6 more genes
    nsv6474423copy number variation1nstd223human GRCh38 chr11: 55,874,701-55,980,800 , GRCh37.p13 chr11: 55,642,177-55,748,276 TRIM51, OR10AK1P, 8 more genes
    nsv6469680copy number variation1nstd223human GRCh38 chr11: 55,890,619-55,891,108 , GRCh37.p13 chr11: 55,658,095-55,658,584 TRIM51
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6294523mobile element insertion1nstd186human GRCh37 chr11: 55,653,810-55,653,861 , GRCh38.p12 chr11: 55,886,334-55,886,385 TRIM51
    nsv6131996copy number variation1nstd213human GRCh37 chr11: 55,349,448-55,758,508 , GRCh38.p12 chr11: 55,581,972-55,991,032 OR5D3P, OR5D2P, 25 more genes
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    nsv5914325copy number variation1nstd209human GRCh38 chr11: 55,273,256-58,053,631 , GRCh37.p13 chr11: 55,040,732-57,821,103 , LOC107984365, 161 more genes
    nsv5909729copy number variation1nstd209human GRCh38 chr11: 55,500,571-56,102,471 , GRCh37.p13 chr11: 55,268,047-55,869,947 OR10AG1, OR5D17P, 37 more genes
    nsv5714117mobile element insertion2nstd211human GRCh38 chr11: 55,886,334-55,886,334 , GRCh37.p13 chr11: 55,653,810-55,653,810 TRIM51
    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