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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5719171mobile element insertion1nstd211human GRCh38 chr6: 159,736,821-159,736,821 , GRCh37.p13 chr6: 160,157,853-160,157,853 WTAP, SOD2
    nsv5685996mobile element insertion1nstd211human GRCh38 chr6: 159,733,181-159,733,181 , GRCh37.p13 chr6: 160,154,213-160,154,213 SOD2, WTAP
    nsv5557765mobile element insertion1nstd206human GRCh38 chr6: 159,736,821-159,736,872 , GRCh37.p13 chr6: 160,157,853-160,157,904 SOD2, WTAP
    nsv5394321mobile element insertion1nstd206human GRCh38 chr6: 159,733,181-159,733,232 , GRCh37.p13 chr6: 160,154,213-160,154,264 SOD2, WTAP
    nsv5310684copy number variation1nstd204human GRCh38.p13 chr6: 159,734,848-159,969,288 , GRCh37.p13 chr6: 160,155,880-160,390,320 SNORA29, SOD2-OT1, 9 more genes
    nsv5236642copy number variation1nstd204human GRCh38.p13 chr6: 159,712,301-159,759,000 , GRCh37.p13 chr6: 160,133,333-160,180,032 SOD2-OT1, SOD2, 3 more genes
    nsv5229894copy number variation1nstd204human GRCh38.p13 chr6: 159,734,717-159,740,911 , GRCh37.p13 chr6: 160,155,749-160,161,943 SOD2, WTAP
    nsv5221863copy number variation1nstd204human GRCh38.p13 chr6: 159,734,701-159,927,700 , GRCh37.p13 chr6: 160,155,733-160,348,732 PNLDC1, SNORA20, 8 more genes
    nsv4824839copy number variation1nstd200human GRCh37 chr6: 160,155,890-160,390,316 , GRCh38.p12 chr6: 159,734,858-159,969,284 SNORA29, MRPL18, 9 more genes
    nsv4766814inversion1nstd199human GRCh37 chr6: 153,752,140-161,206,728 , GRCh38.p12 chr6: 153,431,005-160,785,696 , ACAT2, 111 more genes
    nsv4729113copy number variation1nstd102humanUncertain significance GRCh37 chr6: 159,998,877-160,413,982 , GRCh38.p12 chr6: 159,577,845-159,992,950 PNLDC1, MRPL18, 12 more genes
    nsv4617981copy number variation1nstd183human GRCh37 chr6: 160,131,714-160,147,050 , GRCh38.p12 chr6: 159,710,682-159,726,018 WTAP, HNRNPH1P1, 2 more genes
    nsv4564259mobile element insertion1nstd166human GRCh37.p13 chr6: 160,157,837-160,157,837 , GRCh38.p12 chr6: 159,736,805-159,736,805 WTAP, SOD2
    nsv4523764copy number variation1nstd166human GRCh37.p13 chr6: 160,160,867-160,161,566 , GRCh38.p12 chr6: 159,739,835-159,740,534 WTAP, SOD2
    nsv4481127mobile element insertion1nstd166human GRCh37.p13 chr6: 160,156,079-160,156,079 , GRCh38.p12 chr6: 159,735,047-159,735,047 SOD2, WTAP
    nsv4456598copy number variation1nstd102humanUncertain significance GRCh37 chr6: 160,025,206-160,271,483 , GRCh38.p12 chr6: 159,604,174-159,850,451 SOD2-OT1, RNU4ATAC18P, 10 more genes
    nsv4456177copy number variation1nstd102humanUncertain significance GRCh37 chr6: 160,043,162-160,195,268 , GRCh38.p12 chr6: 159,622,130-159,774,236 ACAT2, SOD2, 4 more genes
    nsv4455446copy number variation1nstd102humanUncertain significance GRCh37 chr6: 157,262,571-160,992,289 , GRCh38.p12 chr6: 156,941,437-160,571,257 LOC105378076, LOC107986663, 67 more genes
    nsv4436131complex substitution1nstd102humanPathogenic GRCh38.p12 chr6: 151,122,197-170,745,979 , GRCh37 chr6: 151,443,333-171,115,067 ACAT2, CCR6, 303 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
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