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 930

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098448copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,181,551-2,192,739 , GRCh38.p12 chr9: 2,181,551-2,192,739 SMARCA2, LOC107987043
    nsv7097968copy number variation1nstd102humanUncertain significance GRCh37 chr9: 676,973-2,729,727 , GRCh38.p12 chr9: 676,973-2,729,727 RN7SL592P, LOC102723803, 23 more genes
    nsv7097716copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,170,399-2,170,492 , GRCh38.p12 chr9: 2,170,399-2,170,492 SMARCA2
    nsv7093292copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,047,296-2,047,379 , GRCh38 chr9: 2,047,296-2,047,379 SMARCA2
    nsv7075424inversion1nstd229human GRCh38 chr9: 2,140,379-2,140,480 , GRCh37.p13 chr9: 2,140,379-2,140,480 SMARCA2
    nsv7073051inversion1nstd229human GRCh38 chr9: 2,083,027-2,090,771 , GRCh37.p13 chr9: 2,083,027-2,090,771 SMARCA2
    nsv7071342inversion1nstd229human GRCh38 chr9: 346,140-2,271,547 , GRCh37.p13 chr9: 346,140-2,271,547 FAM217AP1, DOCK8-AS2, 24 more genes
    nsv7066230inversion1nstd229human GRCh38 chr9: 235,930-9,843,002 , GRCh37.p13 chr9: 235,930-9,843,002 GLIS3-AS1, LOC105375955, 118 more genes
    nsv7065614inversion1nstd229human GRCh38 chr9: 102,865-4,490,246 , GRCh37.p13 chr9: 102,865-4,490,246 RFX3, LOC102723803, 52 more genes
    nsv7064334inversion1nstd229human GRCh38 chr9: 85,493-2,205,560 , GRCh37.p13 chr9: 85,493-2,205,560 FOXD4, LOC105375942, 30 more genes
    nsv6877694copy number variation1nstd229human GRCh38 chr9: 2,186,312-2,186,331 , GRCh37.p13 chr9: 2,186,312-2,186,331 LOC107987043, SMARCA2
    nsv6876527copy number variation1nstd229human GRCh38 chr9: 2,148,201-2,151,500 , GRCh37.p13 chr9: 2,148,201-2,151,500 SMARCA2
    nsv6876124copy number variation1nstd229human GRCh38 chr9: 1,899,095-2,102,631 , GRCh37.p13 chr9: 1,899,095-2,102,631 LOC105375951, SMARCA2, 1 more genes
    nsv6873873copy number variation1nstd229human GRCh38 chr9: 2,084,665-2,160,841 , GRCh37.p13 chr9: 2,084,665-2,160,841 SMARCA2, RNU2-25P
    nsv6872830copy number variation1nstd229human GRCh38 chr9: 2,193,797-2,197,682 , GRCh37.p13 chr9: 2,193,797-2,197,682 LOC107987043, SMARCA2
    nsv6872072copy number variation1nstd229human GRCh38 chr9: 2,176,677-2,177,678 , GRCh37.p13 chr9: 2,176,677-2,177,678 LOC107987043, SMARCA2
    nsv6871475copy number variation1nstd229human GRCh38 chr9: 2,016,721-2,016,834 , GRCh37.p13 chr9: 2,016,721-2,016,834 SMARCA2
    nsv6870486copy number variation1nstd229human GRCh38 chr9: 2,059,180-2,059,288 , GRCh37.p13 chr9: 2,059,180-2,059,288 SMARCA2
    nsv6870234copy number variation1nstd229human GRCh38 chr9: 2,185,285-2,185,338 , GRCh37.p13 chr9: 2,185,285-2,185,338 LOC107987043, SMARCA2
    nsv6870153copy number variation1nstd229human GRCh38 chr9: 2,124,732-2,124,775 , GRCh37.p13 chr9: 2,124,732-2,124,775 SMARCA2
    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