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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
    nsv6912711copy number variation1nstd229human GRCh38 chr11: 46,431,488-46,810,907 , GRCh37.p13 chr11: 46,453,038-46,832,457 AMBRA1, ARHGAP1, 9 more genes
    nsv6903289copy number variation1nstd229human GRCh38 chr11: 46,451,248-46,806,052 , GRCh37.p13 chr11: 46,472,798-46,827,602 CKAP5, ATG13, 9 more genes
    nsv6903029copy number variation1nstd229human GRCh38 chr11: 46,727,780-46,813,902 , GRCh37.p13 chr11: 46,749,330-46,835,452 CKAP5, SNORD67, 2 more genes
    nsv6473242copy number variation1nstd223human GRCh38 chr11: 46,457,965-46,815,552 , GRCh37.p13 chr11: 46,479,515-46,837,102 F2, CKAP5, 7 more genes
    nsv6456787copy number variation1nstd223human GRCh38 chr11: 46,762,688-46,763,112 , GRCh37.p13 chr11: 46,784,238-46,784,662 CKAP5, SNORD67
    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
    nsv6291196copy number variation1nstd102humanPathogenic GRCh37 chr11: 40,117,145-46,920,718 , GRCh38.p12 chr11: 40,095,595-46,899,167 LINC02687, ALKBH3, 86 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
    nsv6132265copy number variation1nstd213human GRCh37 chr11: 46,130,000-46,900,001 , GRCh38.p12 chr11: 46,108,449-46,878,450 ARHGAP1, CHRM4, 23 more genes
    nsv6132108copy number variation1nstd213human GRCh37 chr11: 46,130,000-46,920,001 , GRCh38.p12 chr11: 46,108,449-46,898,450 ARHGAP1, CHRM4, 23 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
    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
    nsv4456633copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,302,171-46,783,079 , GRCh38.p12 chr11: 46,280,620-46,761,529 MIR5582, RPS10P19, 15 more genes
    nsv4210412copy number variation1nstd166human GRCh37.p13 chr11: 46,472,798-46,827,604 , GRCh38.p12 chr11: 46,451,248-46,806,054 HARBI1, AMBRA1, 9 more genes
    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
    nsv3924037copy number variation1nstd102humanUncertain significance NCBI36 chr11: 46,399,070-46,799,238 , GRCh37.p13 chr11: 46,442,494-46,842,662 , GRCh38.p12 chr11: 46,420,944-46,821,111 RPS10P19, AMBRA1, 10 more genes
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