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
    nsv5554173sequence alteration1nstd206human GRCh38 chr8: 18,056,323-18,286,790 , GRCh37.p13 chr8: 17,913,832-18,144,299 NAT1, ASAH1, 5 more genes
    nsv5486385copy number variation1nstd206human GRCh38 chr8: 18,079,405-18,087,893 , GRCh37.p13 chr8: 17,936,914-17,945,402 ASAH1-AS1, ASAH1, 2 more genes
    nsv5481612copy number variation1nstd206human GRCh38 chr8: 18,088,861-18,090,043 , GRCh37.p13 chr8: 17,946,370-17,947,552 ABRAXAS1P2, ASAH1-AS1
    nsv5474153copy number variation1nstd206human GRCh38 chr8: 18,088,746-18,088,874 , GRCh37.p13 chr8: 17,946,255-17,946,383 ASAH1-AS1, ABRAXAS1P2
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4959460copy number variation1nstd200human GRCh38 chr8: 18,088,768-18,090,062 , GRCh37.p13 chr8: 17,946,277-17,947,571 ABRAXAS1P2, ASAH1-AS1
    nsv4959459copy number variation1nstd200human GRCh38 chr8: 18,087,556-18,249,696 , GRCh37.p13 chr8: 17,945,065-18,107,205 ASAH1-AS1, NAT1, 3 more genes
    nsv4959457copy number variation1nstd200human GRCh38 chr8: 18,070,376-18,105,464 , GRCh37.p13 chr8: 17,927,885-17,962,973 ASAH1, ABRAXAS1P2, 2 more genes
    nsv4954213copy number variation1nstd200human GRCh38 chr8: 18,079,425-18,087,873 , GRCh37.p13 chr8: 17,936,934-17,945,382 ABRAXAS1P2, MRPS18CP3, 2 more genes
    nsv4954212copy number variation1nstd200human GRCh38 chr8: 18,067,631-18,560,171 , GRCh37.p13 chr8: 17,925,140-18,417,681 ASAH1-AS1, NAT1, 9 more genes
    nsv4821345copy number variation1nstd200human GRCh37 chr8: 17,945,065-18,107,205 , GRCh38.p12 chr8: 18,087,556-18,249,696 MTND4LP26, ABRAXAS1P2, 3 more genes
    nsv4729680copy number variation1nstd102humanUncertain significance GRCh37 chr8: 17,878,070-18,529,463 , GRCh38.p12 chr8: 18,020,561-18,671,953 NATP, MRPS18CP3, 10 more genes
    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
    nsv4480413mobile element insertion1nstd166human GRCh37.p13 chr8: 17,945,388-17,945,388 , GRCh38.p12 chr8: 18,087,879-18,087,879 MRPS18CP3, ABRAXAS1P2, 1 more genes
    nsv4457323copy number variation1nstd102humanUncertain significance GRCh37 chr8: 17,575,940-18,443,131 , GRCh38.p12 chr8: 17,718,431-18,585,621 ASAH1-AS1, FGL1, 14 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
    nsv4170234copy number variation1nstd166human GRCh37.p13 chr8: 17,946,284-17,947,562 , GRCh38.p12 chr8: 18,088,775-18,090,053 ASAH1-AS1, ABRAXAS1P2
    nsv4166913copy number variation1nstd166human GRCh37.p13 chr8: 17,946,306-17,946,383 , GRCh38.p12 chr8: 18,088,797-18,088,874 ABRAXAS1P2, ASAH1-AS1
    nsv4159187copy number variation1nstd166human GRCh37.p13 chr8: 17,574,000-18,000,000 , GRCh38.p12 chr8: 17,716,491-18,142,491 ASAH1, FGL1, 7 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