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Items: 1 to 20 of 92

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076407inversion1nstd229human GRCh38 chr11: 46,405,448-49,855,596 , GRCh37.p13 chr11: 46,426,998-49,862,647 KBTBD4, MADD-AS1, 89 more genes
    nsv7061528inversion1nstd229human GRCh38 chr11: 47,146,905-49,892,579 , GRCh37.p13 chr11: 47,168,456-49,862,647 YPEL5P2, MADD, 76 more genes
    nsv6908150copy number variation1nstd229human GRCh38 chr11: 47,095,201-47,553,100 , GRCh37.p13 chr11: 47,116,752-47,574,652 ARFGAP2, MIR6745, 15 more genes
    nsv6898317copy number variation1nstd229human GRCh38 chr11: 47,246,952-47,247,476 , GRCh37.p13 chr11: 47,268,503-47,269,027 NR1H3, ACP2
    nsv6469913copy number variation1nstd223human GRCh38 chr11: 47,243,867-47,244,159 , GRCh37.p13 chr11: 47,265,418-47,265,710 ACP2
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6309366copy number variation1nstd102humanPathogenic GRCh37 chr11: 46,880,534-47,470,516 , GRCh38.p12 chr11: 46,858,983-47,448,964 DDB2, PSMC3, 17 more genes
    nsv6132367copy number variation1nstd213human GRCh37 chr11: 46,660,000-47,930,001 , GRCh38.p12 chr11: 46,638,450-47,908,449 ACP2, ARHGAP1, 39 more genes
    nsv6132266copy number variation1nstd213human GRCh37 chr11: 47,180,000-47,890,001 , GRCh38.p12 chr11: 47,158,449-47,868,449 ACP2, DDB2, 28 more genes
    nsv6132180copy number variation1nstd213human GRCh37 chr11: 47,180,000-47,880,001 , GRCh38.p12 chr11: 47,158,449-47,858,449 ACP2, DDB2, 28 more genes
    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
    nsv5380725copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218 MIR4688, LOC112268075, 58 more genes
    nsv4899662mobile element deletion1nstd200human GRCh38 chr11: 47,240,406-47,240,526 , GRCh37.p13 chr11: 47,261,957-47,262,077 ACP2
    nsv4789397mobile element deletion1nstd200human GRCh37 chr11: 47,265,424-47,265,727 , GRCh38.p12 chr11: 47,243,873-47,244,176 ACP2
    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
    nsv4198696copy number variation1nstd166human GRCh37.p13 chr11: 47,262,304-47,263,045 , GRCh38.p12 chr11: 47,240,753-47,241,494 ACP2
    nsv3924778copy number variation1nstd102humanPathogenic GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131 F2, PSMC3, 140 more genes
    nsv3919311copy number variation1nstd102humanPathogenic NCBI36 chr11: 47,188,786-47,405,458 , GRCh37 chr11: 47,232,210-47,448,882 , GRCh38 chr11: 47,210,659-47,427,331 MADD-AS1, PSMC3, 8 more genes
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