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 192

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5196760mobile element insertion1nstd203human GRCh38 chr8: 85,477,582-85,477,591 , GRCh37.p13 chr8: 86,389,811-86,389,820 CA2
    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
    nsv5034498inversion1nstd200human GRCh38 chr8: 85,226,325-85,583,275 , GRCh37.p13 chr8: 86,138,554-86,495,504 , CA1, 6 more genes
    nsv4967550copy number variation1nstd200human GRCh38 chr8: 85,466,305-85,467,061 , GRCh37.p13 chr8: 86,378,534-86,379,290 CA2
    nsv4675773copy number variation1nstd102humanUncertain significance GRCh37 chr8: 85,635,587-86,553,130 , GRCh38.p12 chr8: 84,723,352-85,640,901 CA3, LRRCC1, 16 more genes
    nsv4457216copy number variation1nstd102humanUncertain significance GRCh37 chr8: 84,358,585-89,159,915 , GRCh38.p12 chr8: 83,446,350-88,147,686 LOC100422614, LOC105375933, 61 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456198copy number variation1nstd102humanUncertain significance GRCh37 chr8: 86,358,419-86,494,259 , GRCh38.p12 chr8: 85,446,190-85,582,030 CA3, CA3-AS1, 2 more genes
    nsv4456185copy number variation1nstd102humanUncertain significance GRCh37 chr8: 86,346,299-86,836,910 , GRCh38.p12 chr8: 85,434,070-85,824,681 REXO1L9P, LOC101929627, 14 more genes
    nsv4401038copy number variation1nstd174human GRCh37 chr8: 86,310,570-86,553,130 , GRCh38.p12 chr8: 85,398,341-85,640,901 CA2, LOC105375937, 3 more genes
    nsv4387073copy number variation1nstd173human GRCh37 chr8: 86,382,721-86,533,205 , GRCh38.p12 chr8: 85,470,492-85,620,976 CA2, LOC105375937
    nsv4368272copy number variation1nstd173human GRCh37 chr8: 86,344,443-86,553,141 , GRCh38.p12 chr8: 85,432,214-85,640,912 CA2, CA3-AS1, 3 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
    nsv4332062inversion1nstd166human GRCh37.p13 chr8: 70,438,609-99,073,700 , GRCh38.p12 chr8: 69,526,374-98,061,472 , FTH1P11, 375 more genes
    nsv4318515inversion1nstd166human GRCh37.p13 chr8: 75,861,320-132,789,960 , GRCh38.p12 chr8: 74,949,085-131,777,713 , ANXA13, 716 more genes
    nsv4166577copy number variation1nstd166human GRCh37.p13 chr8: 82,680,857-87,501,720 , GRCh38.p12 chr8: 81,768,622-86,489,491 , REXO1L5P, 58 more genes
    nsv4164210copy number variation1nstd166human GRCh37.p13 chr8: 86,377,796-86,377,890 , GRCh38.p12 chr8: 85,465,567-85,465,661 CA2
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3923011copy number variation1nstd102humanPathogenic GRCh38 chr8: 66,171,669-93,505,509 , GRCh37 chr8: 67,083,904-94,517,737 , NCBI36 chr8: 67,246,458-94,586,913 CA3, HAUS1P3, 353 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