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 172

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5900589copy number variation1nstd209human GRCh38 chr6: 108,221,233-108,221,306 , GRCh37.p13 chr6: 108,542,437-108,542,510 SNX3
    nsv5843645copy number variation1nstd209human GRCh38 chr6: 108,234,224-108,237,557 , GRCh37.p13 chr6: 108,555,428-108,558,761 SNX3
    nsv5578050copy number variation1nstd207human GRCh38 chr6: 108,234,301-108,237,533 , GRCh37.p13 chr6: 108,555,505-108,558,737 SNX3
    nsv5470807copy number variation1nstd206human GRCh38 chr6: 108,221,233-108,221,307 , GRCh37.p13 chr6: 108,542,437-108,542,511 SNX3
    nsv5470528copy number variation1nstd206human GRCh38 chr6: 108,232,819-108,232,923 , GRCh37.p13 chr6: 108,554,023-108,554,127 SNX3
    nsv5466406copy number variation1nstd206human GRCh38 chr6: 108,234,323-108,237,508 , GRCh37.p13 chr6: 108,555,527-108,558,712 SNX3
    nsv5335235translocation1nstd200human GRCh37 chr6: 108,542,437-108,542,437 , GRCh37 chr6: 108,542,511-108,542,511 , GRCh38.p12 chr6: 108,221,233-108,221,233 , GRCh38.p12 chr6: 108,221,307-108,221,307 SNX3
    nsv5236957copy number variation1nstd204human GRCh38.p13 chr6: 108,221,807-108,223,906 , GRCh37.p13 chr6: 108,543,011-108,545,110 SNX3
    nsv5195286mobile element insertion1nstd203human GRCh38 chr6: 108,228,092-108,228,102 , GRCh37.p13 chr6: 108,549,296-108,549,306 SNX3
    nsv5114331mobile element insertion1nstd203human GRCh38 chr6: 108,211,058-108,211,069 , GRCh37.p13 chr6: 108,532,262-108,532,273 SNX3
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4945529copy number variation1nstd200human GRCh38 chr6: 108,182,736-108,261,134 , GRCh37.p13 chr6: 108,503,940-108,582,338 NR2E1, SNX3, 1 more genes
    nsv4942787copy number variation1nstd200human GRCh38 chr6: 108,234,323-108,237,508 , GRCh37.p13 chr6: 108,555,527-108,558,712 SNX3
    nsv4942786copy number variation1nstd200human GRCh38 chr6: 108,219,391-108,220,882 , GRCh37.p13 chr6: 108,540,595-108,542,086 SNX3
    nsv4817460copy number variation1nstd200human GRCh37 chr6: 108,555,526-108,558,713 , GRCh38.p12 chr6: 108,234,322-108,237,509 SNX3
    nsv4768376copy number variation1nstd102humanPathogenic GRCh37 chr6: 98,949,950-114,533,905 , GRCh38.p12 chr6: 98,502,074-114,212,741 LOC101927405, GPR6, 211 more genes
    nsv4734765copy number variation1nstd199human GRCh37 chr6: 108,542,427-108,542,501 , GRCh38.p12 chr6: 108,221,223-108,221,297 SNX3
    nsv4685989copy number variation1nstd102humanPathogenic GRCh37 chr6: 101,287,058-117,013,245 , GRCh38.p12 chr6: 100,839,182-116,692,082 RPL23AP50, RNU6-960P, 216 more genes
    nsv4603021copy number variation1nstd183human GRCh37 chr6: 108,555,471-108,558,690 , GRCh38.p12 chr6: 108,234,267-108,237,486 SNX3
    nsv4571918mobile element insertion1nstd166human GRCh37.p13 chr6: 108,549,296-108,549,296 , GRCh38.p12 chr6: 108,228,092-108,228,092 SNX3
    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