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 144

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5710193mobile element insertion2nstd211human GRCh38 chr15: 49,138,294-49,138,294 , GRCh37.p13 chr15: 49,430,491-49,430,491 COPS2
    nsv5703505mobile element insertion1nstd211human GRCh38 chr15: 49,141,715-49,141,715 , GRCh37.p13 chr15: 49,433,912-49,433,912 COPS2
    nsv5421312mobile element insertion1nstd206human GRCh38 chr15: 49,138,294-49,138,345 , GRCh37.p13 chr15: 49,430,491-49,430,542 COPS2
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5153939mobile element insertion1nstd203human GRCh38 chr15: 49,138,279-49,138,294 , GRCh37.p13 chr15: 49,430,476-49,430,491 COPS2
    nsv5145698mobile element insertion1nstd203human GRCh38 chr15: 49,126,849-49,126,867 , GRCh37.p13 chr15: 49,419,046-49,419,064 COPS2
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005372copy number variation1nstd200human GRCh38 chr15: 49,124,333-49,268,997 , GRCh37.p13 chr15: 49,416,530-49,561,194 MIR4716, COPS2, 4 more genes
    nsv5001713copy number variation1nstd200human GRCh38 chr15: 49,151,379-49,151,980 , GRCh37.p13 chr15: 49,443,576-49,444,177 COPS2
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4866093copy number variation1nstd200human GRCh37 chr15: 49,443,576-49,444,177 , GRCh38.p12 chr15: 49,151,379-49,151,980 COPS2
    nsv4863777copy number variation1nstd200human GRCh37 chr15: 49,416,530-49,561,194 , GRCh38.p12 chr15: 49,124,333-49,268,997 GALK2, MIR4716, 4 more genes
    nsv4769387copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,744,917-53,851,050 , GRCh38.p12 chr15: 48,452,720-53,558,853 BCL2L10, RNA5SP394, 86 more genes
    nsv4675095copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,192,561-50,819,726 , GRCh38.p12 chr15: 46,900,363-50,527,529 LOC102724587, LOC645405, 51 more genes
    nsv4674873copy number variation1nstd102humanUncertain significance GRCh37 chr15: 49,142,668-49,514,861 , GRCh38.p12 chr15: 48,850,471-49,222,664 KRT8P24, EID1, 9 more genes
    nsv4513825mobile element insertion1nstd166human GRCh37.p13 chr15: 49,433,897-49,433,897 , GRCh38.p12 chr15: 49,141,700-49,141,700 COPS2
    nsv4504790mobile element insertion1nstd166human GRCh37.p13 chr15: 49,430,476-49,430,476 , GRCh38.p12 chr15: 49,138,279-49,138,279 COPS2
    nsv4456196copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,000,433-60,747,551 , GRCh38.p12 chr15: 47,708,236-60,455,352 MIR1266, AQP9, 199 more genes
    nsv4455359copy number variation1nstd102humanPathogenic GRCh37 chr15: 49,031,132-56,740,397 , GRCh38.p12 chr15: 48,738,935-56,448,199 MIR4716, RPS13P8, 112 more genes
    nsv4250190copy number variation1nstd166human GRCh37.p13 chr15: 49,432,165-49,432,338 , GRCh38.p12 chr15: 49,139,968-49,140,141 COPS2
    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