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Items: 1 to 20 of 484

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147182insertion1nstd232human GRCh37.p13 chrX: 53,581,883-53,581,883 , GRCh38.p12 chrX: 53,554,922-53,554,922 HUWE1, MIR98
    nsv7147044insertion1nstd232human GRCh37.p13 chrX: 53,579,857-53,579,857 , GRCh38.p12 chrX: 53,552,896-53,552,896 HUWE1
    nsv7144150insertion1nstd232human GRCh37.p13 chrX: 53,589,207-53,589,207 , GRCh38.p12 chrX: 53,562,246-53,562,246 HUWE1
    nsv7140211insertion1nstd232human GRCh37.p13 chrX: 53,562,464-53,562,464 , GRCh38.p12 chrX: 53,535,503-53,535,503 HUWE1
    nsv7138455insertion1nstd232human GRCh37.p13 chrX: 53,572,123-53,572,123 , GRCh38.p12 chrX: 53,545,162-53,545,162 HUWE1
    nsv7137980insertion1nstd232human GRCh37.p13 chrX: 53,566,774-53,566,774 , GRCh38.p12 chrX: 53,539,813-53,539,813 HUWE1
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098540copy number variation1nstd102humanUncertain significance GRCh37 chrX: 53,560,270-53,661,270 , GRCh38.p12 chrX: 53,533,309-53,634,318 HUWE1, MIR98, 1 more genes
    nsv7098539copy number variation1nstd102humanUncertain significance GRCh37 chrX: 53,423,127-53,572,142 , GRCh38.p12 chrX: 53,396,207-53,545,181 MIR6857, RIBC1, 5 more genes
    nsv7098538copy number variation1nstd102humanLikely benign GRCh37 chrX: 53,349,595-53,571,743 , GRCh38.p12 chrX: 53,320,397-53,544,782 SMC1A, HSD17B10, 8 more genes
    nsv7098536copy number variation1nstd102humanUncertain significance GRCh37 chrX: 53,222,149-53,622,383 , GRCh38.p12 chrX: 53,192,967-53,595,423 KDM5C, RIBC1, 13 more genes
    nsv7098323copy number variation1nstd102humanPathogenic GRCh37 chrX: 53,222,149-55,057,617 , GRCh38.p12 chrX: 53,192,967-55,031,184 RPL37P24, KDM5C, 34 more genes
    nsv7091894copy number variation1nstd229human GRCh38 chrX: 53,686,968-53,900,872 , GRCh37.p13 chrX|NW_004070877.1: 3,400,083-3,613,987 , GRCh37.p13 chrX: 53,713,913-53,927,292 HUWE1, MRPS18CP7
    nsv7091893copy number variation1nstd229human GRCh38 chrX: 53,686,201-53,951,900 , GRCh37.p13 chrX: 53,713,146-53,978,333 , GRCh37.p13 chrX|NW_004070877.1: 3,399,316-3,665,015 MRPS18CP7, PHF8, 2 more genes
    nsv7091892copy number variation1nstd229human GRCh38 chrX: 53,684,828-53,730,815 , GRCh37.p13 chrX: 53,711,773-53,757,757 , GRCh37.p13 chrX|NW_004070877.1: 3,397,943-3,443,930 HUWE1
    nsv7091891copy number variation1nstd229human GRCh38 chrX: 53,684,201-53,760,100 , GRCh37.p13 chrX|NW_004070877.1: 3,397,316-3,473,215 , GRCh37.p13 chrX: 53,711,146-53,786,598 HUWE1
    nsv7091890copy number variation1nstd229human GRCh38 chrX: 53,662,985-53,945,531 , GRCh37.p13 chrX|NW_004070877.1: 3,376,100-3,658,646 , GRCh37.p13 chrX: 53,689,939-53,971,964 HUWE1, RNA5SP505, 2 more genes
    nsv7091889copy number variation1nstd229human GRCh38 chrX: 53,653,268-53,654,106 , GRCh37.p13 chrX|NW_004070877.1: 3,366,383-3,367,221 , GRCh37.p13 chrX: 53,680,212-53,681,050 HUWE1
    nsv7091888copy number variation1nstd229human GRCh38 chrX: 53,653,130-53,654,001 , GRCh37.p13 chrX|NW_004070877.1: 3,366,245-3,367,116 , GRCh37.p13 chrX: 53,680,074-53,680,945 HUWE1
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