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 706

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7144219copy number variation1nstd232human GRCh37.p13 chr8: 17,732,990-17,733,095 , GRCh38.p12 chr8: 17,875,481-17,875,586 FGL1
    nsv7097656copy number variation1nstd102humanUncertain significance GRCh37 chr8: 16,850,399-17,885,171 , GRCh38.p12 chr8: 16,992,890-18,027,662 LOC107986919, RPL9P20, 17 more genes
    nsv7071559inversion1nstd229human GRCh38 chr8: 15,858,861-19,517,388 , GRCh37.p13 chr8: 15,716,370-19,374,899 MTMR7, ADAM24P, 45 more genes
    nsv7068901inversion1nstd229human GRCh38 chr8: 17,149,631-17,973,092 , GRCh37.p13 chr8: 17,007,140-17,830,601 SLC7A2, LOC107986918, 15 more genes
    nsv6857696copy number variation1nstd229human GRCh38 chr8: 17,823,573-17,968,458 , GRCh37.p13 chr8: 17,681,082-17,825,967 FGL1, PCM1
    nsv6854607copy number variation1nstd229human GRCh38 chr8: 17,545,688-17,928,879 , GRCh37.p13 chr8: 17,403,197-17,786,388 PDGFRL, SLC7A2, 7 more genes
    nsv6854523copy number variation1nstd229human GRCh38 chr8: 17,865,265-17,872,205 , GRCh37.p13 chr8: 17,722,774-17,729,714 FGL1
    nsv6854428copy number variation1nstd229human GRCh38 chr8: 17,875,510-17,875,589 , GRCh37.p13 chr8: 17,733,019-17,733,098 FGL1
    nsv6854069copy number variation1nstd229human GRCh38 chr8: 17,879,545-17,896,297 , GRCh37.p13 chr8: 17,737,054-17,753,806 FGL1
    nsv6853633copy number variation1nstd229human GRCh38 chr8: 17,804,403-17,937,231 , GRCh37.p13 chr8: 17,661,912-17,794,740 PCM1, MTUS1-DT, 1 more genes
    nsv6853277copy number variation1nstd229human GRCh38 chr8: 17,893,701-17,895,200 , GRCh37.p13 chr8: 17,751,210-17,752,709 FGL1
    nsv6853010copy number variation1nstd229human GRCh38 chr8: 17,881,588-17,892,955 , GRCh37.p13 chr8: 17,739,097-17,750,464 FGL1
    nsv6851811copy number variation1nstd229human GRCh38 chr8: 17,666,115-18,117,017 , GRCh37.p13 chr8: 17,523,624-17,974,526 ASAH1, MIR548V, 8 more genes
    nsv6850992copy number variation1nstd229human GRCh38 chr8: 17,860,682-17,884,451 , GRCh37.p13 chr8: 17,718,191-17,741,960 FGL1
    nsv6849553copy number variation1nstd229human GRCh38 chr8: 17,901,724-17,918,053 , GRCh37.p13 chr8: 17,759,233-17,775,562 FGL1
    nsv6848924copy number variation1nstd229human GRCh38 chr8: 17,860,722-17,884,447 , GRCh37.p13 chr8: 17,718,231-17,741,956 FGL1
    nsv6848665copy number variation1nstd229human GRCh38 chr8: 17,813,778-17,897,260 , GRCh37.p13 chr8: 17,671,287-17,754,769 FGL1, MTUS1-DT
    nsv6848138copy number variation1nstd229human GRCh38 chr8: 17,798,578-17,980,657 , GRCh37.p13 chr8: 17,656,087-17,838,166 FGL1, MTUS1, 2 more genes
    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