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 406

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144251insertion1nstd232human GRCh37.p13 chr9: 102,814,815-102,814,815 , GRCh38.p12 chr9: 100,052,533-100,052,533 ERP44
    nsv7078062inversion1nstd229human GRCh38 chr9: 99,955,191-100,728,757 , GRCh37.p13 chr9: 102,717,473-103,491,039 CAVIN4, UPF3AP3, 13 more genes
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv7071487inversion1nstd229human GRCh38 chr9: 100,005,003-100,009,317 , GRCh37.p13 chr9: 102,767,285-102,771,599 ERP44
    nsv6875991copy number variation1nstd229human GRCh38 chr9: 100,033,224-100,042,548 , GRCh37.p13 chr9: 102,795,506-102,804,830 ERP44
    nsv6873083copy number variation1nstd229human GRCh38 chr9: 100,026,100-100,274,526 , GRCh37.p13 chr9: 102,788,382-103,036,808 ERP44, INVS, 4 more genes
    nsv6867986copy number variation1nstd229human GRCh38 chr9: 100,096,149-100,104,663 , GRCh37.p13 chr9: 102,858,431-102,866,945 RN7SL75P, INVS, 1 more genes
    nsv6866828copy number variation1nstd229human GRCh38 chr9: 100,096,762-100,099,910 , GRCh37.p13 chr9: 102,859,044-102,862,192 ERP44, INVS
    nsv6865753copy number variation1nstd229human GRCh38 chr9: 100,053,834-100,054,034 , GRCh37.p13 chr9: 102,816,116-102,816,316 ERP44
    nsv6865010copy number variation1nstd229human GRCh38 chr9: 100,032,201-100,042,500 , GRCh37.p13 chr9: 102,794,483-102,804,782 ERP44
    nsv6864819copy number variation1nstd229human GRCh38 chr9: 100,077,723-100,082,279 , GRCh37.p13 chr9: 102,840,005-102,844,561 ERP44
    nsv6864749copy number variation1nstd229human GRCh38 chr9: 100,033,223-100,042,552 , GRCh37.p13 chr9: 102,795,505-102,804,834 ERP44
    nsv6863558copy number variation1nstd229human GRCh38 chr9: 100,026,437-100,045,033 , GRCh37.p13 chr9: 102,788,719-102,807,315 LOC105376176, ERP44
    nsv6863112copy number variation1nstd229human GRCh38 chr9: 99,993,337-100,281,635 , GRCh37.p13 chr9: 102,755,619-103,043,917 NANOGP5, LOC105376176, 5 more genes
    nsv6860965copy number variation1nstd229human GRCh38 chr9: 99,996,890-99,996,939 , GRCh37.p13 chr9: 102,759,172-102,759,221 UPF3AP3, ERP44
    nsv6858583copy number variation1nstd229human GRCh38 chr9: 100,023,248-100,024,901 , GRCh37.p13 chr9: 102,785,530-102,787,183 LOC105376176, ERP44
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6565778inversion1nstd223human GRCh38 chr9: 100,005,003-100,009,317 , GRCh37.p13 chr9: 102,767,285-102,771,599 ERP44
    nsv6563128inversion1nstd223human GRCh38 chr9: 100,026,487-100,049,136 , GRCh37.p13 chr9: 102,788,769-102,811,418 LOC105376176, ERP44
    nsv6559721inversion1nstd223human GRCh38 chr9: 100,058,280-100,059,501 , GRCh37.p13 chr9: 102,820,562-102,821,783 ERP44
    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