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 103

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5345396translocation1nstd200human GRCh37 chr21: 15,847,481-15,847,481 , GRCh37 chr21: 15,847,537-15,847,537 , GRCh38.p12 chr21: 14,475,160-14,475,160 , GRCh38.p12 chr21: 14,475,216-14,475,216 , GRCh38.p12 chr21|NW_003315967.2: 63,606-63,606 , GRCh38.p12 chr21|NW_003315967.2: 63,662-63,662 0
    nsv5336555translocation1nstd200human GRCh37 chr21: 15,816,926-15,816,926 , GRCh37 chr21: 15,816,755-15,816,755 , GRCh38.p12 chr21|NW_003315967.2: 33,050-33,050 , GRCh38.p12 chr21: 14,444,434-14,444,434 , GRCh38.p12 chr21: 14,444,605-14,444,605 , GRCh38.p12 chr21|NW_003315967.2: 32,879-32,879 0
    nsv5335328translocation1nstd200human GRCh37 chr21: 15,842,469-15,842,469 , GRCh37 chr21: 15,842,417-15,842,417 , GRCh38.p12 chr21: 14,470,148-14,470,148 , GRCh38.p12 chr21|NW_003315967.2: 58,542-58,542 , GRCh38.p12 chr21: 14,470,096-14,470,096 , GRCh38.p12 chr21|NW_003315967.2: 58,594-58,594 0
    nsv4862551copy number variation1nstd200human GRCh37 chr21: 15,838,009-15,841,627 , GRCh38.p12 chr21|NW_003315967.2: 54,134-57,752 , GRCh38.p12 chr21: 14,465,688-14,469,306 0
    nsv4862550copy number variation1nstd200human GRCh37 chr21: 15,821,684-15,840,027 , GRCh38.p12 chr21: 14,449,363-14,467,706 , GRCh38.p12 chr21|NW_003315967.2: 37,809-56,152 0
    nsv4748034copy number variation1nstd199human GRCh37 chr21: 15,847,470-15,847,535 , GRCh38.p12 chr21: 14,475,149-14,475,214 , GRCh38.p12 chr21|NW_003315967.2: 63,595-63,660 0
    nsv4637776copy number variation2nstd186human GRCh37 chr21: 15,847,481-15,847,537 , GRCh38.p12 chr21: 14,475,160-14,475,216 , GRCh38.p12 chr21|NW_003315967.2: 63,606-63,662 0
    nsv4423438copy number variation1nstd174human GRCh37 chr21: 15,847,462-15,847,543 , GRCh38.p12 chr21|NW_003315967.2: 63,587-63,668 , GRCh38.p12 chr21: 14,475,141-14,475,222 0
    nsv4284366copy number variation1nstd166human GRCh37.p13 chr21: 15,847,481-15,847,537 , GRCh38.p12 chr21|NW_003315967.2: 63,606-63,662 , GRCh38.p12 chr21: 14,475,160-14,475,216 0
    nsv4279442copy number variation1nstd166human GRCh37.p13 chr21: 15,814,030-15,823,774 , GRCh38.p12 chr21|NW_003315967.2: 30,154-39,899 , GRCh38.p12 chr21: 14,441,709-14,451,453 0
    nsv3162438copy number variation1nstd151human GRCh37 chr21: 15,745,935-15,873,061 , GRCh38.p12 chr21|NW_003315967.2: 1-63,917 , GRCh38.p12 chr21: 14,373,614-14,500,740 HSPA13, SAMSN1, 1 more genes
    nsv3069765insertion1nstd90human GRCh37 chr21: 15,811,816-15,811,816 , GRCh38.p12 chr21: 14,439,495-14,439,495 , GRCh38.p12 chr21|NW_003315967.2: 27,940-27,940 0
    nsv3066877insertion1nstd140human GRCh37 chr21: 15,811,808-15,811,808 , GRCh38.p12 chr21: 14,439,487-14,439,487 , GRCh38.p12 chr21|NW_003315967.2: 27,932-27,932 0
    nsv2124820short tandem repeat5nstd128human GRCh37 chr21: 15,839,559-15,839,571 , GRCh38.p12 chr21: 14,467,238-14,467,250 , GRCh38.p12 chr21|NW_003315967.2: 55,684-55,696 0
    nsv2124819short tandem repeat3nstd128human GRCh37 chr21: 15,838,125-15,838,135 , GRCh38.p12 chr21|NW_003315967.2: 54,250-54,260 , GRCh38.p12 chr21: 14,465,804-14,465,814 0
    nsv2124818short tandem repeat4nstd128human GRCh37 chr21: 15,834,332-15,834,362 , GRCh38.p12 chr21: 14,462,011-14,462,041 , GRCh38.p12 chr21|NW_003315967.2: 50,457-50,487 0
    nsv2124817short tandem repeat1nstd128human GRCh37 chr21: 15,831,183-15,831,215 , GRCh38.p12 chr21|NW_003315967.2: 47,308-47,340 , GRCh38.p12 chr21: 14,458,862-14,458,894 0
    nsv2124816short tandem repeat1nstd128human GRCh37 chr21: 15,829,834-15,829,849 , GRCh38.p12 chr21|NW_003315967.2: 45,959-45,974 , GRCh38.p12 chr21: 14,457,513-14,457,528 0
    nsv2124815short tandem repeat1nstd128human GRCh37 chr21: 15,829,072-15,829,095 , GRCh38.p12 chr21: 14,456,751-14,456,774 , GRCh38.p12 chr21|NW_003315967.2: 45,197-45,220 0
    nsv2124814short tandem repeat7nstd128human GRCh37 chr21: 15,825,087-15,825,105 , GRCh38.p12 chr21|NW_003315967.2: 41,212-41,230 , GRCh38.p12 chr21: 14,452,766-14,452,784 0
    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