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 301

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144119insertion1nstd232human GRCh37.p13 chr9: 92,286,478-92,286,478 , GRCh38.p12 chr9: 89,671,563-89,671,563 LINC03062
    nsv7139775insertion1nstd232human GRCh37.p13 chr9: 92,286,457-92,286,457 , GRCh38.p12 chr9: 89,671,542-89,671,542 LINC03062
    nsv7076602inversion1nstd229human GRCh38 chr9: 89,698,816-89,698,890 , GRCh37.p13 chr9|NW_004504301.1: 27,393-27,467 , GRCh37.p13 chr9: 92,313,731-92,313,805 LOC105376140, LINC03062
    nsv7070039inversion1nstd229human GRCh38 chr9: 87,255,950-90,941,993 , GRCh37.p13 chr9: 89,870,865-93,704,275 LOC389768, RPS10P3, 69 more genes
    nsv7066506inversion1nstd229human GRCh38 chr9: 89,677,578-89,683,758 , GRCh37.p13 chr9|NW_004504301.1: 6,155-12,335 , GRCh37.p13 chr9: 92,292,493-92,298,673 LINC03062
    nsv7058174inversion1nstd229human GRCh38 chr9: 89,677,691-89,680,386 , GRCh37.p13 chr9: 92,292,606-92,295,301 , GRCh37.p13 chr9|NW_004504301.1: 6,268-8,963 LINC03062
    nsv6875925copy number variation1nstd229human GRCh38 chr9: 89,684,399-89,690,841 , GRCh37.p13 chr9|NW_004504301.1: 12,976-19,418 , GRCh37.p13 chr9: 92,299,314-92,305,756 LINC03062
    nsv6872684copy number variation1nstd229human GRCh38 chr9: 88,410,189-90,908,033 , GRCh37.p13 chr9: 91,025,104-93,670,315 LOC101927847, IL6RP1, 35 more genes
    nsv6872354copy number variation1nstd229human GRCh38 chr9: 89,641,564-89,641,915 , GRCh37.p13 chr9: 92,256,479-92,256,830 LINC03062
    nsv6870820copy number variation1nstd229human GRCh38 chr9: 89,346,701-89,702,700 , GRCh37.p13 chr9: 91,961,616-92,286,338 LOC105376137, LOC105376140, 6 more genes
    nsv6869392copy number variation1nstd229human GRCh38 chr9: 89,701,001-89,709,400 , GRCh37.p13 chr9|NW_004504301.1: 29,578-37,977 , GRCh37.p13 chr9: 92,315,916-92,324,315 LINC03062, LOC105376140
    nsv6868660copy number variation1nstd229human GRCh38 chr9: 89,693,595-89,693,662 , GRCh37.p13 chr9|NW_004504301.1: 22,172-22,239 , GRCh37.p13 chr9: 92,308,510-92,308,577 LINC03062
    nsv6866975copy number variation1nstd229human GRCh38 chr9: 89,643,716-89,752,946 , GRCh37.p13 chr9|NW_004504301.1: 1-81,523 , GRCh37.p13 chr9: 92,286,339-92,454,393 LINC03062, LOC105376140
    nsv6866974copy number variation1nstd229human GRCh38 chr9: 89,637,740-89,674,966 , GRCh37.p13 chr9: 92,252,655-92,286,338 LINC03062
    nsv6864565copy number variation1nstd229human GRCh38 chr9: 88,599,027-89,704,037 , GRCh37.p13 chr9: 91,213,942-92,286,338 LOC105376135, PCNPP2, 15 more genes
    nsv6863275copy number variation1nstd229human GRCh38 chr9: 89,632,721-89,639,740 , GRCh37.p13 chr9: 92,247,636-92,254,655 LINC03062
    nsv6862552copy number variation1nstd229human GRCh38 chr9: 89,653,788-89,663,095 , GRCh37.p13 chr9: 92,268,703-92,278,010 LINC03062
    nsv6859745copy number variation1nstd229human GRCh38 chr9: 89,685,885-89,692,723 , GRCh37.p13 chr9: 92,300,800-92,307,638 , GRCh37.p13 chr9|NW_004504301.1: 14,462-21,300 LINC03062
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633494copy number variation1nstd224human GRCh37 chr9: 92,260,403-92,526,756 , GRCh38.p12 chr9: 89,645,488-89,825,309 LINC03062, LOC101927823, 2 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