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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5681988mobile element insertion1nstd211human GRCh38 chr4: 127,895,480-127,895,480 , GRCh37.p13 chr4: 128,816,635-128,816,635 PLK4
    nsv5673645copy number variation1nstd102humanPathogenic GRCh37 chr4: 128,544,537-129,131,208 , GRCh38.p12 chr4: 127,623,382-128,210,053 ABHD18, LARP1B, 11 more genes
    nsv5564263copy number variation1nstd102humanUncertain significance GRCh37 chr4: 128,802,290-128,803,101 , GRCh38.p12 chr4: 127,881,135-127,881,946 PLK4
    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
    nsv5458781copy number variation1nstd206human GRCh38 chr4: 127,894,324-127,895,542 , GRCh37.p13 chr4: 128,815,479-128,816,697 PLK4
    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
    nsv5381427copy number variation2nstd102humanUncertain significance GRCh37 chr4: 128,804,417-129,131,208 , GRCh38.p12 chr4: 127,883,262-128,210,053 PLK4, RNU6-583P, 5 more genes
    nsv5381366copy number variation2nstd102humanUncertain significance GRCh37 chr4: 128,554,190-128,886,288 , GRCh38.p12 chr4: 127,633,035-127,965,133 INTU, RPL21P53, 8 more genes
    nsv5199707mobile element insertion1nstd203human GRCh38 chr4: 127,880,917-127,880,933 , GRCh37.p13 chr4: 128,802,072-128,802,088 PLK4
    nsv5086077mobile element insertion1nstd203human GRCh38 chr4: 127,897,824-127,897,858 , GRCh37.p13 chr4: 128,818,979-128,819,013 PLK4
    nsv4935774copy number variation1nstd200human GRCh38 chr4: 127,888,873-128,021,444 , GRCh37.p13 chr4: 128,810,028-128,942,599 MFSD8, ABHD18, 2 more genes
    nsv4792159copy number variation1nstd200human GRCh37 chr4: 128,798,248-128,801,254 , GRCh38.p12 chr4: 127,877,093-127,880,099 PLK4
    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
    nsv4589867copy number variation1nstd183human GRCh37 chr4: 128,819,682-128,820,166 , GRCh38.p12 chr4: 127,898,527-127,899,011 PLK4
    nsv4587294copy number variation1nstd183human GRCh37 chr4: 128,814,762-128,814,833 , GRCh38.p12 chr4: 127,893,607-127,893,678 PLK4
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