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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973701insertion1nstd209human GRCh38 chr11: 62,212,961-62,212,961 , GRCh37.p13 chr11: 61,980,433-61,980,433 SCGB2A1
    nsv5917473copy number variation1nstd209human GRCh38 chr11: 62,209,635-62,237,812 , GRCh37.p13 chr11: 61,977,107-62,005,284 SCGB2A1
    nsv5855953copy number variation1nstd209human GRCh38 chr11: 62,209,444-62,236,971 , GRCh37.p13 chr11: 61,976,916-62,004,443 SCGB2A1
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4985009copy number variation1nstd200human GRCh38 chr11: 62,194,072-62,245,560 , GRCh37.p13 chr11: 61,961,544-62,013,032 SCGB2A1, SCGB1D2
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729555copy number variation1nstd102humanUncertain significance GRCh37 chr11: 61,874,941-62,236,378 , GRCh38.p12 chr11: 62,107,469-62,468,906 INCENP, SCGB2A1, 11 more genes
    nsv4675148copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806 LOC105369326, MS4A18, 91 more genes
    nsv4542819insertion1nstd166human GRCh37.p13 chr11: 61,979,058-61,979,058 , GRCh38.p12 chr11: 62,211,586-62,211,586 SCGB2A1
    nsv4527597copy number variation1nstd166human GRCh37.p13 chr11: 61,981,724-61,981,802 , GRCh38.p12 chr11: 62,214,252-62,214,330 SCGB2A1
    nsv4428093copy number variation1nstd174human GRCh37 chr11: 61,977,592-62,004,945 , GRCh38.p12 chr11: 62,210,120-62,237,473 SCGB2A1
    nsv4205805copy number variation1nstd166human GRCh37.p13 chr11: 61,977,108-62,005,290 , GRCh38.p12 chr11: 62,209,636-62,237,818 SCGB2A1
    nsv3909634copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 61,840,997-62,987,330 , GRCh38.p12 chr11: 62,073,525-63,219,858 CHRM1, EEF1G, 66 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3890886copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 58,935,215-62,177,656 , GRCh38.p12 chr11: 59,167,742-62,410,184 MYRF, TMEM258, 137 more genes
    nsv3168425copy number variation1nstd158human GRCh37 chr11: 3,543,079-67,662,509 , GRCh38.p12 chr11: 3,521,849-67,895,038 , ACP2, 1535 more genes
    nsv3143107copy number variation12nstd151human GRCh37 chr11: 61,977,882-61,981,247 , GRCh38.p12 chr11: 62,210,410-62,213,775 SCGB2A1
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