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 416

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076208inversion1nstd229human GRCh38 chr9: 89,165,687-89,165,722 , GRCh37.p13 chr9: 91,780,602-91,780,637 SHC3
    nsv7070039inversion1nstd229human GRCh38 chr9: 87,255,950-90,941,993 , GRCh37.p13 chr9: 89,870,865-93,704,275 LOC389768, RPS10P3, 69 more genes
    nsv7062482inversion1nstd229human GRCh38 chr9: 89,152,371-89,164,527 , GRCh37.p13 chr9: 91,767,286-91,779,442 SHC3
    nsv6878033copy number variation1nstd229human GRCh38 chr9: 89,160,102-89,166,907 , GRCh37.p13 chr9: 91,775,017-91,781,822 SHC3
    nsv6877331copy number variation1nstd229human GRCh38 chr9: 89,029,594-89,036,544 , GRCh37.p13 chr9: 91,644,509-91,651,459 SHC3
    nsv6875097copy number variation1nstd229human GRCh38 chr9: 89,151,515-89,151,618 , GRCh37.p13 chr9: 91,766,430-91,766,533 SHC3
    nsv6872922copy number variation1nstd229human GRCh38 chr9: 89,039,501-89,064,600 , GRCh37.p13 chr9: 91,654,416-91,679,515 SHC3
    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
    nsv6869796copy number variation1nstd229human GRCh38 chr9: 89,021,410-89,030,005 , GRCh37.p13 chr9: 91,636,325-91,644,920 SHC3
    nsv6869634copy number variation1nstd229human GRCh38 chr9: 89,174,061-89,174,240 , GRCh37.p13 chr9: 91,788,976-91,789,155 SHC3
    nsv6868177copy number variation1nstd229human GRCh38 chr9: 89,028,693-89,028,743 , GRCh37.p13 chr9: 91,643,608-91,643,658 SHC3
    nsv6867866copy number variation1nstd229human GRCh38 chr9: 89,019,936-89,034,278 , GRCh37.p13 chr9: 91,634,851-91,649,193 SHC3
    nsv6867574copy number variation1nstd229human GRCh38 chr9: 89,103,800-89,107,012 , GRCh37.p13 chr9: 91,718,715-91,721,927 SHC3
    nsv6864621copy number variation1nstd229human GRCh38 chr9: 89,112,196-89,161,648 , GRCh37.p13 chr9: 91,727,111-91,776,563 SHC3
    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
    nsv6862803copy number variation1nstd229human GRCh38 chr9: 89,128,801-89,136,500 , GRCh37.p13 chr9: 91,743,716-91,751,415 SHC3
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6567438inversion1nstd223human GRCh38 chr9: 89,136,454-89,138,250 , GRCh37.p13 chr9: 91,751,369-91,753,165 SHC3
    nsv6561678inversion1nstd223human GRCh38 chr9: 89,136,722-89,138,320 , GRCh37.p13 chr9: 91,751,637-91,753,235 SHC3
    nsv6558358inversion1nstd223human GRCh38 chr9: 89,030,543-89,030,842 , GRCh37.p13 chr9: 91,645,458-91,645,757 SHC3
    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