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Items: 1 to 20 of 208

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979503inversion1nstd209human GRCh38 chr12: 131,622,778-131,899,766 , GRCh37.p13 chr12: 132,107,323-132,384,311 MMP17, SFSWAP, 10 more genes
    nsv5974533inversion1nstd209human GRCh38 chr12: 131,540,192-131,862,363 , GRCh37.p13 chr12: 132,024,737-132,346,908 MMP17, SFSWAP, 10 more genes
    nsv5968705inversion1nstd209human GRCh38 chr12: 131,807,431-132,059,968 , GRCh37.p13 chr12: 132,291,976-132,544,513 MMP17, ULK1, 6 more genes
    nsv5930051copy number variation1nstd209human GRCh38 chr12: 131,850,823-131,850,880 , GRCh37.p13 chr12: 132,335,368-132,335,425 MMP17
    nsv5661778insertion1nstd207human GRCh38 chr12: 131,827,357-131,827,357 , GRCh37.p13 chr12: 132,311,902-132,311,902 MMP17
    nsv5561509sequence alteration1nstd206human GRCh38 chr12: 131,746,923-131,837,816 , GRCh37.p13 chr12: 132,231,468-132,322,361 MMP17, SFSWAP, 3 more genes
    nsv5556389sequence alteration1nstd206human GRCh38 chr12: 131,556,124-132,287,086 , GRCh37.p13 chr12: 132,040,669-132,706,992 , ULK1, 25 more genes
    nsv5512935copy number variation1nstd206human GRCh38 chr12: 131,847,382-131,848,307 , GRCh37.p13 chr12: 132,331,927-132,332,852 MMP17
    nsv5507295copy number variation1nstd206human GRCh38 chr12: 131,834,612-131,834,697 , GRCh37.p13 chr12: 132,319,157-132,319,242 MMP17
    nsv5507137copy number variation1nstd206human GRCh38 chr12: 131,843,075-131,848,110 , GRCh37.p13 chr12: 132,327,620-132,332,655 MMP17
    nsv5004262copy number variation1nstd200human GRCh38 chr12: 131,728,030-132,476,582 , GRCh37.p13 chr12: 132,212,575-133,053,168 , LOC105370091, 22 more genes
    nsv4989996copy number variation1nstd200human GRCh38 chr12: 131,834,485-131,834,674 , GRCh37.p13 chr12: 132,319,030-132,319,219 MMP17
    nsv4838090copy number variation1nstd200human GRCh37 chr12: 132,212,575-133,053,168 , GRCh38.p12 chr12: 131,728,030-132,476,582 , LOC105370091, 22 more genes
    nsv4729238copy number variation1nstd102humanUncertain significance GRCh37 chr12: 132,230,559-132,545,601 , GRCh38.p12 chr12: 131,746,014-132,061,056 EP400, LOC105370088, 8 more genes
    nsv4529742copy number variation1nstd166human GRCh37.p13 chr12: 132,308,293-132,311,577 , GRCh38.p12 chr12: 131,823,748-131,827,032 MMP17
    nsv4456888copy number variation1nstd102humanUncertain significance GRCh37 chr12: 126,470,636-133,777,902 , GRCh38.p12 chr12: 125,986,090-133,201,316 LINC02347, LOC107987176, 145 more genes
    nsv4455518copy number variation1nstd102humanUncertain significance GRCh37 chr12: 131,505,849-132,681,966 , GRCh38.p12 chr12: 131,021,304-132,197,421 LOC105370082, LINC02414, 33 more genes
    nsv4436746copy number variation1nstd102humanPathogenic GRCh37 chr12: 131,363,916-133,777,645 , GRCh38.p12 chr12: 130,879,371-133,201,059 LOC107984452, RNA5SP377, 68 more genes
    nsv4422578copy number variation1nstd174human GRCh37 chr12: 132,278,530-132,550,284 , GRCh38.p12 chr12: 131,793,985-132,065,739 SFSWAP, EP400, 8 more genes
    nsv4349911copy number variation1nstd102humanPathogenic GRCh37 chr12: 125,451,405-133,810,935 , GRCh38.p12 chr12: 124,966,859-133,234,349 LOC107987177, GOLGA3, 159 more genes
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