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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5907043copy number variation1nstd209human GRCh38 chr6: 42,082,921-42,082,977 , GRCh37.p13 chr6: 42,050,659-42,050,715 TAF8
    nsv5904111copy number variation1nstd209human GRCh38 chr6: 42,064,882-42,065,286 , GRCh37.p13 chr6: 42,032,620-42,033,024 TAF8
    nsv5686953mobile element insertion1nstd211human GRCh38 chr6: 42,051,203-42,051,203 , GRCh37.p13 chr6: 42,018,941-42,018,941 TAF8
    nsv5570621copy number variation1nstd207human GRCh38 chr6: 42,059,244-42,064,817 , GRCh37.p13 chr6: 42,026,982-42,032,555 TAF8
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5460758copy number variation1nstd206human GRCh38 chr6: 42,059,244-42,064,818 , GRCh37.p13 chr6: 42,026,982-42,032,556 TAF8
    nsv5399715mobile element insertion1nstd206human GRCh38 chr6: 42,051,203-42,051,254 , GRCh37.p13 chr6: 42,018,941-42,018,992 TAF8
    nsv5110069mobile element insertion1nstd203human GRCh38 chr6: 42,064,882-42,064,903 , GRCh37.p13 chr6: 42,032,620-42,032,641 TAF8
    nsv4941095copy number variation1nstd200human GRCh38 chr6: 42,081,215-42,089,035 , GRCh37.p13 chr6: 42,048,953-42,056,773 TAF8
    nsv4941094copy number variation1nstd200human GRCh38 chr6: 42,059,242-42,064,810 , GRCh37.p13 chr6: 42,026,980-42,032,548 TAF8
    nsv4941093copy number variation1nstd200human GRCh38 chr6: 42,049,294-42,052,531 , GRCh37.p13 chr6: 42,017,032-42,020,269 TAF8, CCND3
    nsv4816173copy number variation1nstd200human GRCh37 chr6: 42,017,032-42,020,269 , GRCh38.p12 chr6: 42,049,294-42,052,531 CCND3, TAF8
    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
    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
    nsv4729279copy number variation1nstd102humanLikely benign GRCh37 chr6: 41,922,573-42,024,827 , GRCh38.p12 chr6: 41,954,835-42,057,089 RNU6-761P, CCND3, 2 more genes
    nsv4598590copy number variation1nstd183human GRCh37 chr6: 42,031,235-42,038,962 , GRCh38.p12 chr6: 42,063,497-42,071,224 TAF8
    nsv4598589copy number variation1nstd183human GRCh37 chr6: 42,018,357-42,019,365 , GRCh38.p12 chr6: 42,050,619-42,051,627 TAF8
    nsv4593607copy number variation1nstd183human GRCh37 chr6: 42,002,561-42,059,729 , GRCh38.p12 chr6: 42,034,823-42,091,991 CCND3, TAF8
    nsv4593606copy number variation1nstd183human GRCh37 chr6: 41,976,243-42,019,365 , GRCh38.p12 chr6: 42,008,505-42,051,627 , RNU6-761P, 3 more genes
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