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 257

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5600593copy number variation1nstd207human GRCh38 chr15: 32,595,484-32,595,792 , GRCh37.p13 chr15: 32,887,685-32,887,993 GOLGA8N, ARHGAP11A-DT
    nsv5586173copy number variation1nstd207human GRCh38 chr15: 32,607,506-32,608,059 , GRCh37.p13 chr15: 32,899,707-32,900,260 ARHGAP11A-DT, GOLGA8N
    nsv5504172copy number variation1nstd206human GRCh38 chr15: 32,602,874-32,635,937 , GRCh37.p13 chr15: 32,895,075-32,928,138 ARHGAP11A-SCG5, GOLGA8N, 3 more genes
    nsv5275792copy number variation1nstd204human GRCh38.p13 chr15: 32,605,205-32,629,084 , GRCh37.p13 chr15: 32,897,406-32,921,285 GOLGA8N, ARHGAP11A-SCG5, 2 more genes
    nsv5274409copy number variation1nstd204human GRCh38.p13 chr15: 32,580,701-32,600,500 , GRCh37.p13 chr15: 32,872,902-32,892,701 ARHGAP11A-DT, LINC02256, 2 more genes
    nsv5270072copy number variation1nstd204human GRCh38.p13 chr15: 32,592,401-32,593,400 , GRCh37.p13 chr15: 32,884,602-32,885,601 ARHGAP11A-DT, GOLGA8N
    nsv5263572copy number variation1nstd204human GRCh38.p13 chr15: 32,606,417-32,663,427 , GRCh37.p13 chr15: 32,898,618-32,955,628 GOLGA8N, ARHGAP11A, 3 more genes
    nsv5001134copy number variation1nstd200human GRCh38 chr15: 31,906,597-32,688,706 , GRCh37.p13 chr15: 32,198,800-32,980,907 , DNM1P32, 29 more genes
    nsv4855766copy number variation1nstd200human GRCh37 chr15: 32,198,800-32,980,907 , GRCh38.p12 chr15: 31,906,597-32,688,706 , GRCh38.p12 chr15|NT_187660.1: 2,721,314-4,903,294 , GRCh38.p12 chr15|NW_011332701.1: 4,079,283-4,740,842 , LINC02352, 68 more genes
    nsv4749247copy number variation1nstd199human GRCh37 chr15: 29,159,443-34,700,525 , GRCh38.p12 chr15: 28,914,297-34,408,324 , GRCh38.p12 chr15|NT_187660.1: 1,192,197-5,161,414 , GRCh38.p12 chr15|NW_011332701.1: 1,079,713-4,998,962 , HNRNPA1P71, 132 more genes
    nsv4742703copy number variation1nstd199human GRCh37 chr15: 29,159,443-34,846,747 , GRCh38.p12 chr15: 28,914,297-34,554,546 , GRCh38.p12 chr15|NT_187660.1: 1,192,197-5,161,414 , GRCh38.p12 chr15|NW_011332701.1: 1,079,713-4,998,962 , KATNBL1, 138 more genes
    nsv4729412copy number variation1nstd102humanUncertain significance GRCh37 chr15: 30,386,398-32,915,089 , GRCh38.p12 chr15: 30,094,195-32,622,888 GOLGA8O, LOC105370752, 73 more genes
    nsv4729149copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 28,709,714-34,506,805 , GRCh38.p12 chr15: 28,464,568-34,214,604 APBA2, CHRM5, 125 more genes
    nsv4680904copy number variation1nstd189human GRCh37.p13 chr15: 32,029,433-32,934,730 , GRCh38.p12 chr15: 31,737,230-32,642,529 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-4,857,113 , GRCh38.p12 chr15|NW_011332701.1: 3,909,919-4,694,661 , CHRNA7, 66 more genes
    nsv4680650copy number variation1nstd189human GRCh37.p13 chr15: 31,903,712-32,928,550 , GRCh38.p12 chr15: 31,611,509-32,636,349 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-4,850,933 , GRCh38.p12 chr15|NW_011332701.1: 3,784,208-4,688,481 , CHRNA7, 65 more genes
    nsv4680580copy number variation1nstd189human GRCh37.p13 chr15: 32,049,468-32,928,550 , GRCh38.p12 chr15: 31,757,265-32,636,349 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-4,850,933 , GRCh38.p12 chr15|NW_011332701.1: 3,929,915-4,688,481 , CHRNA7, 65 more genes
    nsv4680042copy number variation1nstd189human GRCh37.p13 chr15: 31,026,704-32,934,730 , GRCh38.p12 chr15: 30,734,501-32,642,529 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-4,857,113 , GRCh38.p12 chr15|NW_011332701.1: 2,907,756-4,694,661 , CHRNA7, 67 more genes
    nsv4679542copy number variation1nstd189human GRCh37.p13 chr15: 32,029,433-32,942,346 , GRCh38.p12 chr15: 31,737,230-32,650,145 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-4,864,727 , GRCh38.p12 chr15|NW_011332701.1: 3,909,919-4,702,275 , CHRNA7, 66 more genes
    nsv4678941copy number variation1nstd189human GRCh37.p13 chr15: 32,049,468-32,942,346 , GRCh38.p12 chr15: 31,757,265-32,650,145 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-4,864,727 , GRCh38.p12 chr15|NW_011332701.1: 3,929,915-4,702,275 , CHRNA7, 66 more genes
    nsv4675702copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,675,452-35,689,958 , GRCh38.p12 chr15: 31,383,249-35,397,757 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-5,161,414 AVEN, PRELID1P4, 113 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