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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924205copy number variation1nstd209human GRCh38 chr11: 43,888,043-43,888,348 , GRCh37.p13 chr11: 43,909,593-43,909,898 ALKBH3
    nsv5923003copy number variation1nstd209human GRCh38 chr11: 43,890,390-43,929,566 , GRCh37.p13 chr11: 43,911,940-43,951,116 SEC14L1P1, ALKBH3-AS1, 1 more genes
    nsv5865348copy number variation1nstd209human GRCh38 chr11: 43,920,557-43,929,724 , GRCh37.p13 chr11: 43,942,107-43,951,274 ALKBH3, ALKBH3-AS1
    nsv5864489copy number variation1nstd209human GRCh38 chr11: 43,890,335-43,901,681 , GRCh37.p13 chr11: 43,911,885-43,923,231 SEC14L1P1, ALKBH3
    nsv5599201copy number variation1nstd207human GRCh38 chr11: 43,888,043-43,888,348 , GRCh37.p13 chr11: 43,909,593-43,909,898 ALKBH3
    nsv5503227copy number variation1nstd206human GRCh38 chr11: 43,888,076-43,888,349 , GRCh37.p13 chr11: 43,909,626-43,909,899 ALKBH3
    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
    nsv5301993copy number variation1nstd204human GRCh38.p13 chr11: 43,888,076-43,888,349 , GRCh37.p13 chr11: 43,909,626-43,909,899 ALKBH3
    nsv5127192mobile element insertion1nstd203human GRCh38 chr11: 43,917,665-43,917,681 , GRCh37.p13 chr11: 43,939,215-43,939,231 ALKBH3, ALKBH3-AS1
    nsv4987242copy number variation1nstd200human GRCh38 chr11: 43,710,265-43,953,275 , GRCh37.p13 chr11: 43,731,815-43,974,825 HSD17B12, ALKBH3, 7 more genes
    nsv4970883copy number variation1nstd200human GRCh38 chr11: 43,888,076-43,888,349 , GRCh37.p13 chr11: 43,909,626-43,909,899 ALKBH3
    nsv4837123copy number variation1nstd200human GRCh37 chr11: 43,909,626-43,909,899 , GRCh38.p12 chr11: 43,888,076-43,888,349 ALKBH3
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4746264copy number variation1nstd199human GRCh37 chr11: 43,909,605-43,909,910 , GRCh38.p12 chr11: 43,888,055-43,888,360 ALKBH3
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729468copy number variation1nstd102humanUncertain significance GRCh37 chr11: 43,223,479-44,266,544 , GRCh38.p12 chr11: 43,201,929-44,244,994 MIR670, ALKBH3, 18 more genes
    nsv4716006copy number variation4nstd195human GRCh37 chr11: 43,909,593-43,909,594 , GRCh38.p12 chr11: 43,888,043-43,888,044 ALKBH3
    nsv4710519copy number variation1nstd195human GRCh37 chr11: 43,800,201-44,412,451 , GRCh38.p12 chr11: 43,778,651-44,390,901 ACCSL, HSD17B12, 9 more genes
    nsv4675989copy number variation1nstd102humanUncertain significance GRCh37 chr11: 43,757,860-44,118,731 , GRCh38.p12 chr11: 43,736,310-44,097,181 SEC14L1P1, EXT2, 8 more genes
    nsv4675717copy number variation1nstd102humanUncertain significance GRCh37 chr11: 43,664,817-44,889,240 , GRCh38.p12 chr11: 43,643,267-44,867,689 C11orf96, ACCSL, 17 more genes
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