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 266

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5674303insertion1nstd102humanPathogenic GRCh37 chr8: 90,995,007-90,995,007 , GRCh38 chr8: 89,982,779-89,982,779 NBN
    nsv5674281insertion1nstd102humanPathogenic GRCh37 chr8: 90,965,538-90,965,538 , GRCh38 chr8: 89,953,310-89,953,310 NBN
    nsv5674058copy number variation1nstd102humanPathogenic GRCh37 chr8: 90,955,471-90,976,745 , GRCh38.p12 chr8: 89,943,243-89,964,517 NBN
    nsv5673871copy number variation1nstd102humanPathogenic GRCh37 chr8: 90,990,438-90,990,561 , GRCh38.p12 chr8: 89,978,210-89,978,333 NBN
    nsv5673870copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 90,970,943-90,971,092 , GRCh38.p12 chr8: 89,958,715-89,958,864 NBN
    nsv5673869copy number variation1nstd102humanPathogenic GRCh37 chr8: 90,958,358-90,960,130 , GRCh38.p12 chr8: 89,946,130-89,947,902 NBN
    nsv5564497copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 90,955,479-90,956,769 , GRCh38 chr8: 89,943,251-89,944,541 NBN
    nsv5485789copy number variation1nstd206human GRCh38 chr8: 89,944,793-89,951,257 , GRCh37.p13 chr8: 90,957,021-90,963,485 NBN
    nsv5381481copy number variation1nstd102humanUncertain significance GRCh37 chr8: 90,944,564-90,997,899 , GRCh38.p12 chr8: 89,932,336-89,985,671 OSGIN2, NBN
    nsv5112781mobile element insertion1nstd203human GRCh38 chr8: 89,948,460-89,948,474 , GRCh37.p13 chr8: 90,960,688-90,960,702 NBN
    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
    nsv4952496copy number variation1nstd200human GRCh38 chr8: 89,932,191-89,941,895 , GRCh37.p13 chr8: 90,944,419-90,954,123 OSGIN2, NBN
    nsv4729552copy number variation1nstd102humanUncertain significance GRCh37 chr8: 88,194,550-91,779,543 , GRCh38.p12 chr8: 87,182,322-90,767,315 RIPK2, RNU6-925P, 29 more genes
    nsv4683716copy number variation1nstd102humanUncertain significance GRCh37 chr8: 90,947,800-90,976,745 , GRCh38.p12 chr8: 89,935,572-89,964,517 NBN, OSGIN2
    nsv4683208copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 90,958,358-90,958,533 , GRCh38.p12 chr8: 89,946,130-89,946,305 NBN
    nsv4682916copy number variation1nstd102humanUncertain significance GRCh37 chr8: 90,947,269-91,064,145 , GRCh38.p12 chr8: 89,935,041-90,051,917 DECR1, NBN, 1 more genes
    nsv4682855copy number variation1nstd102humanUncertain significance GRCh37 chr8: 90,990,438-90,996,789 , GRCh38.p12 chr8: 89,978,210-89,984,561 NBN
    nsv4682442copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr8: 90,947,810-90,996,789 , GRCh38.p12 chr8: 89,935,582-89,984,561 OSGIN2, NBN
    nsv4682248copy number variation1nstd102humanPathogenic GRCh37 chr8: 90,992,952-90,996,799 , GRCh38.p12 chr8: 89,980,724-89,984,571 NBN
    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