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 184

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955955insertion1nstd209human GRCh38 chr4: 122,899,044-122,899,044 , GRCh37.p13 chr4: 123,820,199-123,820,199 NUDT6
    nsv5689138mobile element insertion1nstd211human GRCh38 chr4: 122,921,130-122,921,130 , GRCh37.p13 chr4: 123,842,285-123,842,285 AFG2A, NUDT6
    nsv5683451mobile element insertion2nstd211human GRCh38 chr4: 122,913,781-122,913,781 , GRCh37.p13 chr4: 123,834,936-123,834,936 NUDT6
    nsv5673739copy number variation1nstd102humanPathogenic GRCh37 chr4: 123,663,028-124,235,239 , GRCh38.p12 chr4: 122,741,873-123,314,084 FGF2, NUDT6, 5 more genes
    nsv5577432copy number variation1nstd207human GRCh38 chr4: 122,900,205-122,900,357 , GRCh37.p13 chr4: 123,821,360-123,821,512 NUDT6
    nsv5575109copy number variation1nstd207human GRCh38 chr4: 122,919,514-122,921,129 , GRCh37.p13 chr4: 123,840,669-123,842,284 AFG2A, NUDT6
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5558253sequence alteration1nstd206human GRCh38 chr4: 120,373,769-143,797,136 , GRCh37.p13 chr4: 121,294,924-144,718,289 , IL15, 218 more genes
    nsv5467622copy number variation1nstd206human GRCh38 chr4: 122,919,295-122,921,183 , GRCh37.p13 chr4: 123,840,450-123,842,338 AFG2A, NUDT6
    nsv5401537mobile element insertion1nstd206human GRCh38 chr4: 122,913,781-122,913,832 , GRCh37.p13 chr4: 123,834,936-123,834,987 NUDT6
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 LOC112268469, LOC105377393, 159 more genes
    nsv5237674copy number variation1nstd204human GRCh38.p13 chr4: 122,892,085-122,893,308 , GRCh37.p13 chr4: 123,813,240-123,814,463 FGF2, NUDT6
    nsv5232889copy number variation1nstd204human GRCh38.p13 chr4: 122,892,209-122,897,441 , GRCh37.p13 chr4: 123,813,364-123,818,596 NUDT6, FGF2
    nsv5098324mobile element insertion1nstd203human GRCh38 chr4: 122,913,766-122,913,781 , GRCh37.p13 chr4: 123,834,921-123,834,936 NUDT6
    nsv4935656copy number variation1nstd200human GRCh38 chr4: 122,919,340-122,921,139 , GRCh37.p13 chr4: 123,840,495-123,842,294 NUDT6, AFG2A
    nsv4935655copy number variation1nstd200human GRCh38 chr4: 122,918,676-122,919,959 , GRCh37.p13 chr4: 123,839,831-123,841,114 NUDT6
    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
    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