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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975420inversion1nstd209human GRCh38 chr4: 44,594,542-44,748,679 , GRCh37.p13 chr4: 44,596,559-44,750,696 GUF1, GNPDA2, 2 more genes
    nsv5687476mobile element insertion2nstd211human GRCh38 chr4: 44,709,750-44,709,750 , GRCh37.p13 chr4: 44,711,767-44,711,767 GNPDA2
    nsv5685533mobile element insertion1nstd211human GRCh38 chr4: 44,722,360-44,722,360 , GRCh37.p13 chr4: 44,724,377-44,724,377 GNPDA2
    nsv5413687mobile element insertion1nstd206human GRCh38 chr4: 44,709,750-44,709,801 , GRCh37.p13 chr4: 44,711,767-44,711,818 GNPDA2
    nsv5409504mobile element insertion1nstd206human GRCh38 chr4: 44,722,360-44,722,411 , GRCh37.p13 chr4: 44,724,377-44,724,428 GNPDA2
    nsv5344193translocation1nstd200human GRCh37 chr4: 44,706,138-44,706,138 , GRCh37 chr4: 44,706,540-44,706,540 , GRCh38.p12 chr4: 44,704,523-44,704,523 , GRCh38.p12 chr4: 44,704,121-44,704,121 GNPDA2
    nsv5334297translocation1nstd200human GRCh37 chr4: 44,706,113-44,706,113 , GRCh37 chr4: 44,704,152-44,704,152 , GRCh38.p12 chr4: 44,702,135-44,702,135 , GRCh38.p12 chr4: 44,704,096-44,704,096 GNPDA2
    nsv5332296translocation1nstd200human GRCh37 chr4: 44,706,504-44,706,504 , GRCh37 chr4: 44,704,151-44,704,151 , GRCh38.p12 chr4: 44,704,487-44,704,487 , GRCh38.p12 chr4: 44,702,134-44,702,134 GNPDA2
    nsv5326535translocation1nstd204human GRCh38.p13 chr4: 44,704,096-44,704,096 , GRCh38.p13 chr4: 44,702,135-44,702,135 , GRCh37.p13 chr4: 44,704,152-44,704,152 , GRCh37.p13 chr4: 44,706,113-44,706,113 GNPDA2
    nsv5326259translocation1nstd204human GRCh38.p13 chr4: 44,704,523-44,704,523 , GRCh38.p13 chr4: 44,704,121-44,704,121 , GRCh37.p13 chr4: 44,706,138-44,706,138 , GRCh37.p13 chr4: 44,706,540-44,706,540 GNPDA2
    nsv5323987translocation1nstd204human GRCh38.p13 chr4: 44,702,134-44,702,134 , GRCh38.p13 chr4: 44,704,487-44,704,487 , GRCh37.p13 chr4: 44,704,151-44,704,151 , GRCh37.p13 chr4: 44,706,504-44,706,504 GNPDA2
    nsv5228113copy number variation1nstd204human GRCh38.p13 chr4: 44,701,759-44,704,158 , GRCh37.p13 chr4: 44,703,776-44,706,175 GNPDA2
    nsv5226327copy number variation1nstd204human GRCh38.p13 chr4: 44,715,301-44,719,800 , GRCh37.p13 chr4: 44,717,318-44,721,817 GNPDA2
    nsv5090074mobile element insertion1nstd203human GRCh38 chr4: 44,709,740-44,709,750 , GRCh37.p13 chr4: 44,711,757-44,711,767 GNPDA2
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4928623copy number variation1nstd200human GRCh38 chr4: 44,710,013-44,710,305 , GRCh37.p13 chr4: 44,712,030-44,712,322 GNPDA2
    nsv4791657copy number variation1nstd200human GRCh37 chr4: 44,714,098-44,714,589 , GRCh38.p12 chr4: 44,712,081-44,712,572 GNPDA2
    nsv4791656copy number variation1nstd200human GRCh37 chr4: 44,712,030-44,712,322 , GRCh38.p12 chr4: 44,710,013-44,710,305 GNPDA2
    nsv4791614copy number variation1nstd200human GRCh37 chr4: 43,358,175-53,119,711 , GRCh38.p12 chr4: 43,356,158-52,253,545 , LOC107986277, 78 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
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