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 412

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5709009mobile element insertion1nstd211human GRCh38 chr8: 26,845,148-26,845,148 , GRCh37.p13 chr8: 26,702,665-26,702,665 ADRA1A
    nsv5699755mobile element insertion2nstd211human GRCh38 chr8: 26,813,003-26,813,003 , GRCh37.p13 chr8: 26,670,520-26,670,520 ADRA1A
    nsv5629801insertion1nstd207human GRCh38 chr8: 26,812,993-26,812,993 , GRCh37.p13 chr8: 26,670,510-26,670,510 ADRA1A
    nsv5491324copy number variation1nstd206human GRCh38 chr8: 26,736,109-26,736,506 , GRCh37.p13 chr8: 26,593,626-26,594,023 ADRA1A
    nsv5490617copy number variation1nstd206human GRCh38 chr8: 26,737,606-26,747,334 , GRCh37.p13 chr8: 26,595,123-26,604,851 ADRA1A
    nsv5488920copy number variation1nstd206human GRCh38 chr8: 26,742,500-26,742,884 , GRCh37.p13 chr8: 26,600,017-26,600,401 ADRA1A
    nsv5480888copy number variation1nstd206human GRCh38 chr8: 26,789,360-26,789,424 , GRCh37.p13 chr8: 26,646,877-26,646,941 ADRA1A
    nsv5301526copy number variation1nstd204human GRCh38.p13 chr8: 26,785,868-26,785,940 , GRCh37.p13 chr8: 26,643,385-26,643,457 ADRA1A
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5119962mobile element insertion1nstd203human GRCh38 chr8: 26,845,138-26,845,148 , GRCh37.p13 chr8: 26,702,655-26,702,665 ADRA1A
    nsv5114256mobile element insertion1nstd203human GRCh38 chr8: 26,812,997-26,813,003 , GRCh37.p13 chr8: 26,670,514-26,670,520 ADRA1A
    nsv5113254mobile element insertion1nstd203human GRCh38 chr8: 26,812,993-26,813,003 , GRCh37.p13 chr8: 26,670,510-26,670,520 ADRA1A
    nsv4959814copy number variation1nstd200human GRCh38 chr8: 26,825,454-26,826,441 , GRCh37.p13 chr8: 26,682,971-26,683,958 ADRA1A
    nsv4959813copy number variation1nstd200human GRCh38 chr8: 26,785,873-26,785,936 , GRCh37.p13 chr8: 26,643,390-26,643,453 ADRA1A
    nsv4959812copy number variation1nstd200human GRCh38 chr8: 26,772,154-26,774,481 , GRCh37.p13 chr8: 26,629,671-26,631,998 ADRA1A, RPLP1P9
    nsv4959811copy number variation1nstd200human GRCh38 chr8: 26,754,278-26,759,609 , GRCh37.p13 chr8: 26,611,795-26,617,126 ADRA1A
    nsv4959810copy number variation1nstd200human GRCh38 chr8: 26,737,606-26,747,334 , GRCh37.p13 chr8: 26,595,123-26,604,851 ADRA1A
    nsv4821579copy number variation1nstd200human GRCh37 chr8: 26,694,521-26,694,911 , GRCh38.p12 chr8: 26,837,004-26,837,394 ADRA1A
    nsv4821578copy number variation1nstd200human GRCh37 chr8: 26,668,950-26,670,375 , GRCh38.p12 chr8: 26,811,433-26,812,858 ADRA1A
    nsv4821577copy number variation1nstd200human GRCh37 chr8: 26,643,390-26,643,453 , GRCh38.p12 chr8: 26,785,873-26,785,936 ADRA1A
    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