U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Nucleotide

Items: 1 to 20 of 926

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145448copy number variation1nstd232human GRCh37.p13 chr15: 22,933,654-22,933,743 , GRCh38.p12 chr15: 22,939,325-22,939,414 , GRCh38.p12 chr15|NT_187603.1: 36,354-36,443 CYFIP1
    nsv6637675copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-23,082,328 , GRCh38.p12 chr15: 22,790,740-23,102,646 , GRCh38.p12 chr15|NT_187603.1: 1-202,805 NIPA1, ELMO2P1, 3 more genes
    nsv6637453copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-23,082,442 , GRCh38.p12 chr15: 22,790,626-23,102,646 , GRCh38.p12 chr15|NT_187603.1: 1-202,805 CYFIP1, NIPA2, 3 more genes
    nsv6635732copy number variation1nstd227human GRCh38.p12 chr15: 22,600,363-23,220,738 , GRCh37 chr15: 22,652,330-23,272,733 , GRCh38.p12 chr15|NT_187603.1: 1-321,246 CYFIP1, ABCB10P1, 20 more genes
    nsv6622837copy number variation1nstd224human GRCh37 chr15: 22,770,994-22,842,081 , GRCh38.p12 chr15: 23,030,987-23,102,074 , GRCh38.p12 chr15|NT_187659.1: 1-71,584 , GRCh38.p12 chr15|NT_187603.1: 128,005-202,233 ELMO2P1, TUBGCP5
    nsv6622622copy number variation1nstd224human GRCh37 chr15: 22,770,994-23,086,929 , GRCh38.p12 chr15: 22,786,139-23,102,074 , GRCh38.p12 chr15|NT_187603.1: 1-202,233 TUBGCP5, NIPA1, 3 more genes
    nsv6622621copy number variation1nstd224human GRCh37 chr15: 22,766,739-22,801,026 , GRCh38.p12 chr15: 23,072,042-23,106,329 , GRCh38.p12 chr15|NT_187659.1: 41,552-75,839 , GRCh38.p12 chr15|NT_187603.1: 172,205-206,808 ELMO2P1
    nsv6315489copy number variation1nstd102humanUncertain significance GRCh37 chr15: 22,770,421-23,005,425 , GRCh38.p12 chr15|NT_187603.1: 1-202,806 , GRCh38.p12 chr15: 22,867,643-23,102,647 ELMO2P1, NIPA2, 2 more genes
    nsv6315467copy number variation2nstd102humanUncertain significance GRCh37 chr15: 22,770,421-23,082,328 , GRCh38.p12 chr15: 22,790,740-23,102,647 , GRCh38.p12 chr15|NT_187603.1: 1-202,806 CYFIP1, NIPA1, 3 more genes
    nsv6291777copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 22,811,927-23,082,442 , GRCh38.p12 chr15: 22,790,626-23,061,141 , GRCh38.p12 chr15|NT_187603.1: 1-161,139 CYFIP1, NIPA2, 2 more genes
    nsv6132946copy number variation1nstd213human GRCh37 chr15: 22,750,000-23,150,001 , GRCh38.p12 chr15: 22,723,105-23,123,068 , GRCh38.p12 chr15|NT_187603.1: 1-223,576 CYFIP1, TUBGCP5, 8 more genes
    nsv6131292insertion1nstd186human GRCh37 chr15: 22,769,075-22,769,075 , GRCh38.p12 chr15|NT_187603.1: 204,152-204,152 , GRCh38.p12 chr15: 23,103,993-23,103,993 , GRCh38.p12 chr15|NT_187659.1: 73,503-73,503 0
    nsv6130438insertion1nstd186human GRCh37 chr15: 22,797,866-22,797,866 , GRCh38.p12 chr15|NT_187603.1: 175,365-175,365 , GRCh38.p12 chr15|NT_187659.1: 44,712-44,712 , GRCh38.p12 chr15: 23,075,202-23,075,202 0
    nsv6129815insertion1nstd186human GRCh37 chr15: 22,909,567-22,909,622 , GRCh38.p12 chr15: 22,963,446-22,963,501 , GRCh38.p12 chr15|NT_187603.1: 60,499-60,547 CYFIP1
    nsv6116262copy number variation1nstd186human GRCh37 chr15: 22,831,102-22,832,240 , GRCh38.p12 chr15|NT_187603.1: 139,668-140,651 , GRCh38.p12 chr15: 23,040,828-23,041,966 0
    nsv6114852mobile element insertion1nstd186human GRCh37 chr15: 22,896,440-22,896,469 , GRCh38.p12 chr15: 22,976,599-22,976,628 , GRCh38.p12 chr15|NT_187603.1: 73,606-73,635 CYFIP1
    nsv6114019copy number variation1nstd186human GRCh37 chr15: 22,650,826-22,709,826 , GRCh38.p12 chr15: 23,163,242-23,222,242 , GRCh38.p12 chr15|NT_187659.1: 132,752-191,752 , GRCh38.p12 chr15|NT_187603.1: 263,750-322,750 ABCB10P1, GOLGA8DP, 2 more genes
    nsv5389825copy number variation1nstd186human GRCh37 chr15: 22,823,187-22,832,225 , GRCh38.p12 chr15: 23,040,843-23,049,881 , GRCh38.p12 chr15|NT_187603.1: 139,682-149,879 0
    nsv5345665translocation1nstd200human GRCh37 chr3: 48,533,403-48,533,403 , GRCh37 chr15: 22,943,472-22,943,472 , GRCh38.p9 chr: NaN-NaN , GRCh38.p12 chr15: 22,929,596-22,929,596 , GRCh38.p12 chr: NaN-NaN , GRCh38.p12 chr15|NT_187603.1: 26,619-26,619 CYFIP1
    nsv5200374copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,765,628-23,085,096 , GRCh38.p12 chr15: 22,787,972-23,107,440 , GRCh38.p12 chr15|NT_187603.1: 1-207,919 TUBGCP5, NIPA1, 3 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