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 197

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5711481mobile element insertion2nstd211human GRCh38 chr8: 117,522,711-117,522,711 , GRCh37.p13 chr8: 118,534,950-118,534,950 MED30, RPS10P16
    nsv5711079mobile element insertion1nstd211human GRCh38 chr8: 117,524,307-117,524,307 , GRCh37.p13 chr8: 118,536,546-118,536,546 MED30
    nsv5413547mobile element insertion1nstd206human GRCh38 chr8: 117,522,711-117,522,762 , GRCh37.p13 chr8: 118,534,950-118,535,001 MED30, RPS10P16
    nsv5408815mobile element insertion1nstd206human GRCh38 chr8: 117,524,307-117,524,358 , GRCh37.p13 chr8: 118,536,546-118,536,597 MED30
    nsv5118570mobile element insertion1nstd203human GRCh38 chr8: 117,540,699-117,540,725 , GRCh37.p13 chr8: 118,552,938-118,552,964 MED30
    nsv5117869mobile element insertion1nstd203human GRCh38 chr8: 117,522,700-117,522,711 , GRCh37.p13 chr8: 118,534,939-118,534,950 RPS10P16, MED30
    nsv5106222mobile element insertion1nstd203human GRCh38 chr8: 117,522,705-117,522,711 , GRCh37.p13 chr8: 118,534,944-118,534,950 MED30, RPS10P16
    nsv5105343mobile element insertion1nstd203human GRCh38 chr8: 117,522,706-117,522,711 , GRCh37.p13 chr8: 118,534,945-118,534,950 RPS10P16, MED30
    nsv5101832mobile element insertion1nstd203human GRCh38 chr8: 117,522,701-117,522,711 , GRCh37.p13 chr8: 118,534,940-118,534,950 RPS10P16, MED30
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4967722copy number variation1nstd200human GRCh38 chr8: 117,535,807-117,547,902 , GRCh37.p13 chr8: 118,548,046-118,560,141 MED30
    nsv4827825copy number variation1nstd200human GRCh37 chr8: 118,548,046-118,560,141 , GRCh38.p12 chr8: 117,535,807-117,547,902 MED30
    nsv4729586copy number variation1nstd102humanUncertain significance GRCh37 chr8: 118,513,760-118,636,771 , GRCh38.p12 chr8: 117,501,521-117,624,532 MED30, RPS10P16, 2 more genes
    nsv4729071copy number variation1nstd102humanPathogenic GRCh37 chr8: 108,421,573-123,429,638 , GRCh38.p12 chr8: 107,409,345-122,417,399 RN7SL396P, LOC107986970, 124 more genes
    nsv4675535copy number variation1nstd102humanPathogenic GRCh37 chr8: 118,466,438-119,966,333 , GRCh38.p12 chr8: 117,454,199-118,954,094 SAMD12, LOC105375716, 12 more genes
    nsv4675222copy number variation1nstd102humanPathogenic GRCh37 chr8: 111,514,791-123,192,373 , GRCh38.p12 chr8: 110,502,562-122,180,134 LOC105375723, CSMD3, 93 more genes
    nsv4674902copy number variation1nstd102humanUncertain significance GRCh37 chr8: 118,214,380-118,884,778 , GRCh38.p12 chr8: 117,202,141-117,872,539 EXT1, LOC105375721, 5 more genes
    nsv4612710copy number variation1nstd183human GRCh37 chr8: 118,547,945-118,552,592 , GRCh38.p12 chr8: 117,535,706-117,540,353 MED30
    nsv4601524copy number variation1nstd183human GRCh37 chr8: 118,552,288-118,552,585 , GRCh38.p12 chr8: 117,540,049-117,540,346 MED30
    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