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 144

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094385copy number variation2nstd102humanPathogenic GRCh37 chr15: 50,999,997-54,025,330 , GRCh38.p12 chr15: 50,707,800-53,733,133 LOC105370826, MIR7973-2, 48 more genes
    nsv7094384copy number variation1nstd102humanUncertain significance GRCh37 chr15: 50,731,271-54,025,330 , GRCh38.p12 chr15: 50,439,074-53,733,133 LOC105370823, TMOD3, 54 more genes
    nsv7073585inversion1nstd229human GRCh38 chr15: 52,093,790-52,249,452 , GRCh37.p13 chr15: 52,385,987-52,541,649 GNB5, BCL2L10, 5 more genes
    nsv7065242inversion1nstd229human GRCh38 chr15: 52,093,673-52,247,548 , GRCh37.p13 chr15: 52,385,870-52,539,745 BCL2L10, CERNA1, 5 more genes
    nsv7059635inversion1nstd229human GRCh38 chr15: 51,716,761-55,548,818 , GRCh37.p13 chr15: 52,008,958-55,841,016 CCPG1, LOC105370823, 51 more genes
    nsv7059534inversion1nstd229human GRCh38 chr15: 51,726,660-55,605,328 , GRCh37.p13 chr15: 52,018,857-55,897,526 HNRNPA1P74, MYO5C, 50 more genes
    nsv6974313copy number variation1nstd229human GRCh38 chr15: 52,068,601-52,324,700 , GRCh37.p13 chr15: 52,360,798-52,616,897 RPS13P8, LOC112268150, 8 more genes
    nsv6966546copy number variation1nstd229human GRCh38 chr15: 52,104,766-52,107,677 , GRCh37.p13 chr15: 52,396,963-52,399,874 BCL2L10
    nsv6966374copy number variation1nstd229human GRCh38 chr15: 52,082,901-52,181,000 , GRCh37.p13 chr15: 52,375,098-52,473,197 LOC112268150, BCL2L10, 3 more genes
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6623268copy number variation1nstd224human GRCh37 chr15: 52,356,136-52,412,563 , GRCh38.p12 chr15: 52,063,939-52,120,366 MAPK6, LOC112268150, 3 more genes
    nsv6511814copy number variation1nstd223human GRCh38 chr15: 52,104,810-52,107,649 , GRCh37.p13 chr15: 52,397,007-52,399,846 BCL2L10
    nsv6510767copy number variation1nstd223human GRCh38 chr15: 52,096,885-52,138,128 , GRCh37.p13 chr15: 52,389,082-52,430,325 BCL2L10, LOC112268150, 1 more genes
    nsv6313917copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,635,238-56,509,908 , GRCh38.p12 chr15: 47,343,041-56,217,710 PYGO1, RNU6-449P, 125 more genes
    nsv6132897copy number variation1nstd213human GRCh37 chr15: 50,000,000-53,730,001 , GRCh38.p12 chr15: 49,707,803-53,437,804 MAPK6, ARPP19, 65 more genes
    nsv5942626copy number variation1nstd209human GRCh38 chr15: 52,104,739-52,107,648 , GRCh37.p13 chr15: 52,396,936-52,399,845 BCL2L10
    nsv5856640copy number variation1nstd209human GRCh38 chr15: 52,104,773-52,107,662 , GRCh37.p13 chr15: 52,396,970-52,399,859 BCL2L10
    nsv5598621copy number variation1nstd207human GRCh38 chr15: 52,104,739-52,107,648 , GRCh37.p13 chr15: 52,396,936-52,399,845 BCL2L10
    nsv5533695copy number variation1nstd206human GRCh38 chr15: 52,104,613-52,107,649 , GRCh37.p13 chr15: 52,396,810-52,399,846 BCL2L10
    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
    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