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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5710853mobile element insertion1nstd211human GRCh38 chr18: 47,163,940-47,163,940 , GRCh37.p13 chr18: 44,690,311-44,690,311 IER3IP1
    nsv5555886sequence alteration1nstd206human GRCh37.p13 chr18: 44,617,345-44,857,797 , GRCh38 chr18: 47,090,974-47,331,426 IER3IP1, KATNAL2, 6 more genes
    nsv5522581copy number variation1nstd206human GRCh38 chr18: 47,172,221-47,172,329 , GRCh37.p13 chr18: 44,698,592-44,698,700 IER3IP1
    nsv5415461mobile element insertion1nstd206human GRCh38 chr18: 47,163,940-47,163,991 , GRCh37.p13 chr18: 44,690,311-44,690,362 IER3IP1
    nsv5381046copy number variation2nstd102humanUncertain significance GRCh37 chr18: 42,281,312-45,423,127 , GRCh38.p12 chr18: 44,701,347-47,896,756 HDHD2, RNU6-1131P, 45 more genes
    nsv5359076translocation1nstd200human GRCh38 chr18: 47,172,221-47,172,221 , GRCh38 chr18: 47,172,329-47,172,329 , GRCh37.p13 chr18: 44,698,700-44,698,700 , GRCh37.p13 chr18: 44,698,592-44,698,592 IER3IP1
    nsv5357122translocation1nstd200human GRCh38 chr18: 47,167,450-47,167,450 , GRCh38 chr14: 39,063,758-39,063,758 , GRCh37.p13 chr18: 44,693,821-44,693,821 , GRCh37.p13 chr14: 39,532,962-39,532,962 SEC23A, IER3IP1
    nsv5149221mobile element insertion1nstd203human GRCh38 chr18: 47,167,961-47,167,974 , GRCh37.p13 chr18: 44,694,332-44,694,345 IER3IP1
    nsv4859538copy number variation1nstd200human GRCh37 chr18: 44,698,592-44,698,700 , GRCh38.p12 chr18: 47,172,221-47,172,329 IER3IP1
    nsv4676219copy number variation1nstd102humanPathogenic GRCh37 chr18: 41,630,585-45,107,905 , GRCh38.p12 chr18: 44,050,620-47,581,534 HAUS1, KATNAL2, 48 more genes
    nsv4676155copy number variation1nstd102humanPathogenic GRCh37 chr18: 20,689,919-49,455,212 , GRCh38.p12 chr18: 23,109,955-51,928,842 KLHL14, RPL23AP77, 318 more genes
    nsv4625941copy number variation1nstd183human GRCh37 chr18: 44,564,162-44,759,488 , GRCh38.p12 chr18: 47,037,791-47,233,117 IER3IP1, KATNAL2, 5 more genes
    nsv4457774copy number variation1nstd102humanUncertain significance GRCh37 chr18: 44,552,637-44,765,469 , GRCh38.p12 chr18: 47,026,266-47,239,098 KATNAL2, RNU6-1131P, 7 more genes
    nsv4457507copy number variation1nstd102humanUncertain significance GRCh37 chr18: 44,619,805-46,854,791 , GRCh38.p12 chr18: 47,093,434-49,328,421 LOC105372105, CTIF, 29 more genes
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    nsv4262355copy number variation1nstd166human GRCh37.p13 chr18: 44,698,592-44,698,700 , GRCh38.p12 chr18: 47,172,221-47,172,329 IER3IP1
    nsv4259028copy number variation1nstd166human GRCh37.p13 chr18: 44,688,846-44,689,268 , GRCh38.p12 chr18: 47,162,475-47,162,897 IER3IP1
    nsv3924706copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097 LOC100420948, NPM1P2, 941 more genes
    nsv3924638copy number variation1nstd102humanPathogenic GRCh38 chr18: 20,962,119-74,691,446 , NCBI36 chr18: 16,796,078-70,532,390 , GRCh37 chr18: 18,542,080-72,403,402 HMGN1P30, LOC107985134, 596 more genes
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