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 193

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5493063copy number variation1nstd206human GRCh38 chr8: 17,490,010-17,737,534 , GRCh37.p13 chr8: 17,347,519-17,595,043 PDGFRL, SLC7A2, 3 more genes
    nsv5475245copy number variation1nstd206human GRCh38 chr8: 17,676,732-17,680,150 , GRCh37.p13 chr8: 17,534,241-17,537,659 MTUS1, MIR548V
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4959428copy number variation1nstd200human GRCh38 chr8: 17,676,732-17,680,150 , GRCh37.p13 chr8: 17,534,241-17,537,659 MIR548V, MTUS1
    nsv4959427copy number variation1nstd200human GRCh38 chr8: 17,656,851-17,680,202 , GRCh37.p13 chr8: 17,514,360-17,537,711 MTUS1, MIR548V
    nsv4954206copy number variation1nstd200human GRCh38 chr8: 17,530,701-17,861,635 , GRCh37.p13 chr8: 17,388,210-17,719,144 MTUS1, RNA5SP256, 5 more genes
    nsv4821318copy number variation1nstd200human GRCh37 chr8: 17,534,241-17,537,659 , GRCh38.p12 chr8: 17,676,732-17,680,150 MIR548V, MTUS1
    nsv4728911copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,528,482-29,886,483 , GRCh38.p12 chr8: 12,670,973-30,028,967 NAT1, NAT2, 272 more genes
    nsv4456885copy number variation1nstd102humanUncertain significance GRCh37 chr8: 17,487,884-17,883,260 , GRCh38.p12 chr8: 17,630,375-18,025,751 PCM1, MTUS1, 5 more genes
    nsv4456647copy number variation1nstd102humanUncertain significance GRCh37 chr8: 17,474,031-17,883,039 , GRCh38.p12 chr8: 17,616,522-18,025,530 PDGFRL, MIR548V, 5 more genes
    nsv4455568copy number variation1nstd102humanUncertain significance GRCh37 chr8: 17,465,054-17,864,004 , GRCh38.p12 chr8: 17,607,545-18,006,495 MIR548V, MTUS1-DT, 6 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4348018copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,546,855-35,816,855 , GRCh38.p12 chr8: 12,689,346-35,959,337 NAT1, NAT2, 343 more genes
    nsv4166003copy number variation1nstd166human GRCh37.p13 chr8: 17,534,241-17,537,659 , GRCh38.p12 chr8: 17,676,732-17,680,150 MTUS1, MIR548V
    nsv4164148copy number variation1nstd166human GRCh37.p13 chr8: 17,214,122-17,809,601 , GRCh38.p12 chr8: 17,356,613-17,952,092 RNA5SP256, PDGFRL, 10 more genes
    nsv4157601copy number variation1nstd166human GRCh37.p13 chr8: 16,579,053-17,873,572 , GRCh38.p12 chr8: 16,721,544-18,016,063 MICU3, MIR548V, 19 more genes
    nsv4157202copy number variation1nstd166human GRCh37.p13 chr8: 17,426,253-17,619,592 , GRCh38.p12 chr8: 17,568,744-17,762,083 PDGFRL, SLC7A2, 4 more genes
    nsv4153945copy number variation1nstd166human GRCh37.p13 chr8: 17,388,243-17,719,102 , GRCh38.p12 chr8: 17,530,734-17,861,593 PDGFRL, SLC7A2, 5 more genes
    nsv3972390copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,556,004-34,374,150 , GRCh38.p12 chr8: 12,698,495-34,516,632 NAT1, NAT2, 335 more genes
    nsv3924532copy number variation1nstd102humanPathogenic NCBI36 chr8: 181,605-31,068,132 , GRCh38 chr8: 241,605-31,091,074 , GRCh37 chr8: 191,605-30,948,590 DEFB109B, GATA4, 585 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