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 108

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969033inversion1nstd209human GRCh38 chr4: 108,267,752-117,667,772 , GRCh37.p13 chr4: 109,188,908-118,588,927 , ANK2, 134 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5462773copy number variation1nstd206human GRCh38 chr4: 112,028,273-112,074,115 , GRCh37.p13 chr4: 112,949,429-112,995,271 CCDC34P1
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4943846copy number variation1nstd200human GRCh38 chr4: 111,940,715-112,165,400 , GRCh37.p13 chr4: 112,861,871-113,086,556 RPS12P8, CCDC34P1, 3 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4794400copy number variation1nstd200human GRCh37 chr4: 112,861,871-113,086,556 , GRCh38.p12 chr4: 111,940,715-112,165,400 FAM241A, LOC105377370, 3 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4729714copy number variation1nstd102humanPathogenic GRCh37 chr4: 111,334,313-113,223,858 , GRCh38.p12 chr4: 110,413,157-112,302,702 PANCR, LOC105377369, 20 more genes
    nsv4521005copy number variation1nstd166human GRCh37.p13 chr4: 111,349,997-113,150,000 , GRCh38.p12 chr4: 110,428,841-112,228,844 , RPL36AP23, 17 more genes
    nsv4374635copy number variation1nstd173human GRCh37 chr4: 111,109,020-113,950,046 , GRCh38.p12 chr4: 110,187,864-113,028,890 , HSBP1P2, 52 more genes
    nsv4342697sequence alteration1nstd166human GRCh37.p13 chr4: 73,901,505-160,870,682 , GRCh38.p12 chr4: 73,035,788-159,949,530 , ADH1B, 1083 more genes
    nsv4328272inversion1nstd166human GRCh37.p13 chr4: 110,343,023-114,944,660 , GRCh38.p12 chr4: 109,421,867-114,023,504 , EGF, 82 more genes
    nsv4111764copy number variation1nstd166human GRCh37.p13 chr4: 112,967,000-113,009,000 , GRCh38.p12 chr4: 112,045,844-112,087,844 TUBB8P3, CCDC34P1
    nsv3920388copy number variation1nstd102humanPathogenic GRCh37 chr4: 97,014,044-137,331,362 , NCBI36 chr4: 97,233,067-137,550,812 , GRCh38 chr4: 96,092,893-136,410,207 MIR576, ABT1P1, 447 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