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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5505868copy number variation1nstd206human GRCh38 chr14: 20,686,383-20,707,077 , GRCh37.p13 chr14: 21,154,542-21,175,236 RNASE4, ANG
    nsv5503825copy number variation1nstd206human GRCh38 chr14: 20,701,090-20,706,399 , GRCh37.p13 chr14: 21,169,249-21,174,558 RNASE4
    nsv5301230copy number variation1nstd204human GRCh38.p13 chr14: 20,674,268-20,693,618 , GRCh37.p13 chr14: 21,142,427-21,161,777 ANG, RNASE4, 4 more genes
    nsv5277038copy number variation1nstd204human GRCh37.p13 chr14: 21,142,506-21,161,783 , GRCh38.p13 chr14: 20,674,347-20,693,624 ANG, RNASE4, 4 more genes
    nsv5147372mobile element insertion1nstd203human GRCh38 chr14: 20,690,221-20,690,247 , GRCh37.p13 chr14: 21,158,380-21,158,406 ANG, RNASE4
    nsv4994076copy number variation1nstd200human GRCh38 chr14: 20,701,114-20,706,573 , GRCh37.p13 chr14: 21,169,273-21,174,732 RNASE4
    nsv4994075copy number variation1nstd200human GRCh38 chr14: 20,658,530-20,710,223 , GRCh37.p13 chr14: 21,126,689-21,178,382 , ANG, 7 more genes
    nsv4994069copy number variation1nstd200human GRCh38 chr14: 20,462,869-20,801,429 , GRCh37.p13 chr14: 20,931,028-21,269,588 , RNASE9, 34 more genes
    nsv4990720copy number variation1nstd200human GRCh38 chr14: 20,701,231-20,706,470 , GRCh37.p13 chr14: 21,169,390-21,174,629 RNASE4
    nsv4990719copy number variation1nstd200human GRCh38 chr14: 20,701,083-20,705,555 , GRCh37.p13 chr14: 21,169,242-21,173,714 RNASE4
    nsv4990718copy number variation1nstd200human GRCh38 chr14: 20,690,043-20,707,233 , GRCh37.p13 chr14: 21,158,202-21,175,392 ANG, RNASE4
    nsv4990717copy number variation1nstd200human GRCh38 chr14: 20,689,517-20,693,053 , GRCh37.p13 chr14: 21,157,676-21,161,212 RNASE4, ANG
    nsv4844049copy number variation1nstd200human GRCh37 chr14: 21,169,268-21,174,744 , GRCh38.p12 chr14: 20,701,109-20,706,585 RNASE4
    nsv4839816copy number variation1nstd200human GRCh37 chr14: 21,169,359-21,174,644 , GRCh38.p12 chr14: 20,701,200-20,706,485 RNASE4
    nsv4832225copy number variation1nstd200human GRCh37 chr14: 21,169,242-21,173,714 , GRCh38.p12 chr14: 20,701,083-20,705,555 RNASE4
    nsv4729394copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-21,915,516 , GRCh38.p12 chr14: 20,043,513-21,447,357 SETP1, OR11H5P, 99 more genes
    nsv4729177copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,109,252-21,182,930 , GRCh38.p12 chr14: 20,641,093-20,714,771 RNASE4, TRL-TAG4-1, 9 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
    nsv4676085copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,143,933-23,297,667 , GRCh38.p12 chr14: 20,675,774-22,828,458 ANG, SNORD8, 209 more genes
    nsv4675977copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 21,159,605-22,252,320 , GRCh38.p12 chr14: 20,691,446-21,784,103 ANG, HNRNPC, 69 more genes
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