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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918104copy number variation1nstd209human GRCh38 chr11: 104,190,618-110,044,159 , GRCh37.p13 chr11: 104,061,346-109,914,884 , CARD18, 71 more genes
    nsv5700906mobile element insertion1nstd211human GRCh38 chr11: 106,078,232-106,078,232 , GRCh37.p13 chr11: 105,948,959-105,948,959 KBTBD3, AASDHPPT
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5511629copy number variation1nstd206human GRCh38 chr11: 106,080,927-106,085,387 , GRCh37.p13 chr11: 105,951,654-105,956,114 AASDHPPT
    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
    nsv5186585mobile element insertion1nstd203human GRCh38 chr11: 106,083,793-106,083,812 , GRCh37.p13 chr11: 105,954,520-105,954,539 AASDHPPT
    nsv4706973copy number variation1nstd195human GRCh37 chr11: 105,829,401-105,993,301 , GRCh38.p12 chr11: 105,958,674-106,122,574 GRIA4, AASDHPPT, 4 more genes
    nsv4676052copy number variation1nstd102humanUncertain significance GRCh37 chr11: 103,980,525-106,914,369 , GRCh38.p12 chr11: 104,109,797-107,043,643 CARD17P, LOC643855, 36 more genes
    nsv4675680copy number variation1nstd102humanPathogenic GRCh37 chr11: 103,320,065-114,349,787 , GRCh38.p12 chr11: 103,449,337-114,479,065 DRD2, NCAM1, 181 more genes
    nsv4675323copy number variation1nstd102humanPathogenic GRCh37 chr11: 105,699,599-114,524,876 , GRCh38.p12 chr11: 105,828,873-114,654,154 RPSAP50, RNA5SP349, 155 more genes
    nsv4675179copy number variation1nstd102humanUncertain significance GRCh37 chr11: 105,875,295-106,313,332 , GRCh38.p12 chr11: 106,004,568-106,442,605 LOC643855, MSANTD4, 5 more genes
    nsv4675055copy number variation1nstd102humanUncertain significance GRCh37 chr11: 103,983,847-106,914,369 , GRCh38.p12 chr11: 104,113,119-107,043,643 LOC105369466, CASP4LP, 36 more genes
    nsv4539123insertion1nstd166human GRCh37.p13 chr11: 105,964,342-105,964,342 , GRCh38.p12 chr11: 106,093,615-106,093,615 AASDHPPT
    nsv4502942mobile element insertion1nstd166human GRCh37.p13 chr11: 105,950,079-105,950,079 , GRCh38.p12 chr11: 106,079,352-106,079,352 AASDHPPT
    nsv4455554copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202 LINC02732, LINC02698, 198 more genes
    nsv4455453copy number variation1nstd102humanUncertain significance GRCh37 chr11: 105,875,296-106,210,917 , GRCh38.p12 chr11: 106,004,569-106,340,190 LOC101928535, AASDHPPT, 4 more genes
    nsv4212345copy number variation1nstd166human GRCh37.p13 chr11: 105,885,000-106,313,400 , GRCh38.p12 chr11: 106,014,273-106,442,673 AASDHPPT, MSANTD4, 5 more genes
    nsv3922253copy number variation1nstd102humanPathogenic GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246 RPS27P19, UBASH3B, 655 more genes
    nsv3922086copy number variation1nstd102humanPathogenic GRCh38 chr11: 104,142,626-107,019,997 , NCBI36 chr11: 103,518,564-106,395,933 , GRCh37 chr11: 104,013,354-106,890,723 LOC105369468, CASP1, 36 more genes
    nsv3913977copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356 PLS1P1, SNORA25, 349 more genes
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