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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5890291copy number variation1nstd209human GRCh38 chr6: 43,067,621-43,068,289 , GRCh37.p13 chr6: 43,035,359-43,036,027 KLC4
    nsv5677481mobile element insertion1nstd211human GRCh38 chr6: 43,070,111-43,070,111 , GRCh37.p13 chr6: 43,037,849-43,037,849 KLC4
    nsv5673766copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,928,506-43,737,486 , GRCh38.p12 chr6: 42,960,768-43,769,749 SRF, POLR1C, 39 more genes
    nsv5565822copy number variation1nstd207human GRCh38 chr6: 43,067,813-43,068,138 , GRCh37.p13 chr6: 43,035,551-43,035,876 KLC4
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5464428copy number variation1nstd206human GRCh38 chr6: 43,067,805-43,068,139 , GRCh37.p13 chr6: 43,035,543-43,035,877 KLC4
    nsv5383922mobile element deletion1nstd186human GRCh37 chr6: 43,035,568-43,035,856 , GRCh38.p12 chr6: 43,067,830-43,068,118 KLC4
    nsv5383785mobile element deletion1nstd186human GRCh37 chr6: 43,035,568-43,035,850 , GRCh38.p12 chr6: 43,067,830-43,068,112 KLC4
    nsv5302794copy number variation1nstd204human GRCh38.p13 chr6: 43,067,766-43,068,317 , GRCh37.p13 chr6: 43,035,504-43,036,055 KLC4
    nsv4934681copy number variation1nstd200human GRCh38 chr6: 43,066,013-43,165,563 , GRCh37.p13 chr6: 43,033,751-43,133,301 PTK7, KLC4, 1 more genes
    nsv4934680copy number variation1nstd200human GRCh38 chr6: 43,062,268-43,064,109 , GRCh37.p13 chr6: 43,030,006-43,031,847 KLC4
    nsv4880598mobile element deletion1nstd200human GRCh38 chr6: 43,067,830-43,068,118 , GRCh37.p13 chr6: 43,035,568-43,035,856 KLC4
    nsv4828671copy number variation1nstd200human GRCh37 chr6: 43,033,751-43,133,301 , GRCh38.p12 chr6: 43,066,013-43,165,563 KLC4-AS1, PTK7, 1 more genes
    nsv4778609mobile element deletion1nstd200human GRCh37 chr6: 43,035,473-43,035,942 , GRCh38.p12 chr6: 43,067,735-43,068,204 KLC4
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4737994copy number variation1nstd199human GRCh37 chr6: 43,035,558-43,035,885 , GRCh38.p12 chr6: 43,067,820-43,068,147 KLC4
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4592683copy number variation1nstd183human GRCh37 chr6: 42,627,455-43,357,404 , GRCh38.p12 chr6: 42,659,717-43,389,666 , PEX6, 36 more genes
    nsv4411633copy number variation1nstd174human GRCh37 chr6: 43,035,317-43,035,902 , GRCh38.p12 chr6: 43,067,579-43,068,164 KLC4
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