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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5510321copy number variation1nstd206human GRCh38 chr14: 28,781,359-28,781,444 , GRCh37.p13 chr14: 29,250,565-29,250,650 LINC01551
    nsv5506696copy number variation1nstd206human GRCh38 chr14: 28,776,938-28,777,543 , GRCh37.p13 chr14: 29,246,144-29,246,749 LINC01551
    nsv5498410copy number variation1nstd206human GRCh38 chr14: 28,780,474-28,780,974 , GRCh37.p13 chr14: 29,249,680-29,250,180 LINC01551
    nsv5497752copy number variation1nstd206human GRCh38 chr14: 28,786,706-28,786,803 , GRCh37.p13 chr14: 29,255,912-29,256,009 LINC01551
    nsv5381770copy number variation1nstd102humanPathogenic GRCh37 chr14: 27,450,705-31,529,481 , GRCh38.p12 chr14: 26,981,499-31,060,275 RPS27AP4, LINC00645, 43 more genes
    nsv5374469translocation1nstd200human GRCh38 chr14: 28,805,920-28,805,920 , GRCh38 chr14: 28,793,584-28,793,584 , GRCh37.p13 chr14: 29,262,790-29,262,790 , GRCh37.p13 chr14: 29,275,126-29,275,126 LINC01551, LINC02281
    nsv5357046translocation1nstd200human GRCh38 chr14: 28,780,974-28,780,974 , GRCh38 chr14: 28,780,474-28,780,474 , GRCh37.p13 chr14: 29,250,180-29,250,180 , GRCh37.p13 chr14: 29,249,680-29,249,680 LINC01551
    nsv5303460copy number variation1nstd204human GRCh38.p13 chr14: 28,780,468-28,780,977 , GRCh37.p13 chr14: 29,249,674-29,250,183 LINC01551
    nsv5039802inversion1nstd200human GRCh38 chr14: 28,794,897-28,805,927 , GRCh37.p13 chr14: 29,264,103-29,275,133 LINC01551, LINC02281
    nsv4991059copy number variation1nstd200human GRCh38 chr14: 28,793,584-28,794,848 , GRCh37.p13 chr14: 29,262,790-29,264,054 LINC01551, LINC02281
    nsv4991058copy number variation1nstd200human GRCh38 chr14: 28,786,706-28,786,803 , GRCh37.p13 chr14: 29,255,912-29,256,009 LINC01551
    nsv4872874inversion1nstd200human GRCh37 chr14: 29,264,103-29,275,133 , GRCh38.p12 chr14: 28,794,897-28,805,927 LINC01551, LINC02281
    nsv4831777copy number variation1nstd200human GRCh37 chr14: 29,249,680-29,250,180 , GRCh38.p12 chr14: 28,780,474-28,780,974 LINC01551
    nsv4829794copy number variation1nstd200human GRCh37 chr14: 29,255,912-29,256,009 , GRCh38.p12 chr14: 28,786,706-28,786,803 LINC01551
    nsv4769384copy number variation1nstd102humanPathogenic GRCh37 chr14: 28,836,918-29,955,663 , GRCh38.p12 chr14: 28,367,712-29,486,457 LINC02327, EIF4A1P12, 15 more genes
    nsv4729530copy number variation1nstd102humanPathogenic GRCh37 chr14: 25,172,628-30,285,023 , GRCh38.p12 chr14: 24,703,422-29,815,817 LINC02281, RNU6-864P, 42 more genes
    nsv4685750copy number variation1nstd102humannot provided GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685 IGBP1P1, RAB2B, 579 more genes
    nsv4675943copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827 TRAJ36, SEC23A-AS1, 590 more genes
    nsv4457072copy number variation1nstd102humanPathogenic GRCh37 chr14: 28,484,920-29,691,434 , GRCh38.p12 chr14: 28,015,714-29,222,228 RNU6-864P, LINC02281, 15 more genes
    nsv4455189copy number variation1nstd102humanPathogenic GRCh37 chr14: 27,735,516-30,451,857 , GRCh38.p12 chr14: 27,266,310-29,982,651 LINC02281, BTF3P2, 22 more genes
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