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Items: 1 to 20 of 437

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077192inversion1nstd229human GRCh38 chr22: 26,758,160-26,763,214 , GRCh37.p13 chr22: 27,154,123-27,159,177 MIATNB
    nsv7073094inversion1nstd229human GRCh38 chr22: 22,618,607-30,089,219 , GRCh37.p13 chr22: 22,961,077-30,485,208 BCRP1, POM121L10P, 237 more genes
    nsv7062396inversion1nstd229human GRCh38 chr22: 26,687,905-26,689,269 , GRCh37.p13 chr22: 27,083,868-27,085,232 MIATNB
    nsv7060877inversion1nstd229human GRCh38 chr22: 26,753,999-26,763,326 , GRCh37.p13 chr22: 27,149,962-27,159,289 MIATNB
    nsv7036641copy number variation1nstd229human GRCh38 chr22: 26,756,906-26,756,937 , GRCh37.p13 chr22: 27,152,869-27,152,900 MIATNB
    nsv7033060copy number variation1nstd229human GRCh38 chr22: 26,693,884-26,694,069 , GRCh37.p13 chr22: 27,089,847-27,090,032 MIATNB
    nsv7031974copy number variation1nstd229human GRCh38 chr22: 26,727,676-26,731,123 , GRCh37.p13 chr22: 27,123,639-27,127,086 MIATNB
    nsv7030341copy number variation1nstd229human GRCh38 chr22: 26,683,101-26,689,300 , GRCh37.p13 chr22: 27,079,064-27,085,263 MIATNB
    nsv7028873copy number variation1nstd229human GRCh38 chr22: 22,977,123-28,064,565 , GRCh37.p13 chr22: 23,319,297-28,460,553 LOC100652871, VPREB3, 132 more genes
    nsv7027574copy number variation1nstd229human GRCh38 chr22: 26,713,259-26,715,174 , GRCh37.p13 chr22: 27,109,222-27,111,137 MIATNB
    nsv7026864copy number variation1nstd229human GRCh38 chr22: 26,721,369-26,733,977 , GRCh37.p13 chr22: 27,117,332-27,129,940 MIATNB
    nsv7025646copy number variation1nstd229human GRCh38 chr22: 26,733,812-26,738,211 , GRCh37.p13 chr22: 27,129,775-27,134,174 MIATNB
    nsv7022233copy number variation1nstd229human GRCh38 chr22: 26,695,814-26,695,854 , GRCh37.p13 chr22: 27,091,777-27,091,817 MIATNB
    nsv7021353copy number variation1nstd229human GRCh38 chr22: 26,703,699-26,703,808 , GRCh37.p13 chr22: 27,099,662-27,099,771 MIATNB
    nsv7020487copy number variation1nstd229human GRCh38 chr22: 26,733,813-26,741,963 , GRCh37.p13 chr22: 27,129,776-27,137,926 MIATNB
    nsv7018682copy number variation1nstd229human GRCh38 chr22: 26,694,679-26,695,078 , GRCh37.p13 chr22: 27,090,642-27,091,041 MIATNB
    nsv6637977copy number variation1nstd102humanPathogenic GRCh37 chr22: 26,614,429-29,847,680 , GRCh38.p12 chr22: 26,218,463-29,451,691 MIAT, LOC105372985, 65 more genes
    nsv6596913inversion1nstd223human GRCh38 chr22: 22,928,460-27,825,377 , GRCh37.p13 chr22: 23,270,636-28,221,365 LOC105372957, LOC105372980, 126 more genes
    nsv6596101inversion1nstd223human GRCh38 chr22: 26,682,923-26,688,259 , GRCh37.p13 chr22: 27,078,886-27,084,222 MIATNB
    nsv6596080inversion1nstd223human GRCh38 chr22: 26,754,961-26,756,430 , GRCh37.p13 chr22: 27,150,924-27,152,393 MIATNB
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