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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4674327copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,475,385-23,764,120 , GRCh38.p12 chr22: 17,992,619-23,421,933 ESS2, GP1BB, 308 more genes
    nsv3917936copy number variation1nstd102humanPathogenic NCBI36 chr22: 18,659,766-22,152,986 , GRCh38 chr22: 18,339,130-23,480,799 , GRCh37 chr22: 20,279,766-23,822,986 ESS2, IGLV7-46, 298 more genes
    nsv4676119copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-20,730,144 , GRCh38.p12 chr22: 16,408,173-20,375,854 ESS2, C22orf39, 150 more genes
    nsv3923978copy number variation1nstd102humanPathogenic NCBI36 chr22: 15,399,015-19,048,227 , GRCh37 chr22: 17,019,015-20,718,227 , GRCh38 chr22: 16,538,125-20,363,937 ESS2, MIR185, 146 more genes
    nsv4676296copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-20,125,005 , GRCh38.p12 chr22: 16,408,173-20,137,482 ESS2, FAM230J, 139 more genes
    nsv3895935copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,900-20,026,751 , GRCh38.p12 chr22: 16,408,174-20,039,228 ESS2, FAM247C, 131 more genes
    nsv3913197copy number variation2nstd102humanPathogenic GRCh37 chr22: 17,397,498-20,708,934 , GRCh38 chr22: 16,916,608-20,354,644 , NCBI36 chr22: 15,777,498-19,038,934 ESS2, E2F6P1, 128 more genes
    nsv3910919copy number variation2nstd102humanPathogenic NCBI36 chr22: 15,777,498-18,691,763 , GRCh37 chr22: 17,397,498-20,311,763 , GRCh38 chr22: 16,916,608-20,324,240 ESS2, C22orf39, 127 more genes
    nsv3901351copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,644,790-21,915,509 , GRCh38.p12 chr22: 18,162,023-21,561,220 ESS2, RPL34P35, 149 more genes
    nsv6634411copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,639,780-21,910,280 , GRCh38.p12 chr22: 18,157,013-21,555,991 ESS2, RIMBP3C, 149 more genes
    nsv3912933copy number variation1nstd102humanPathogenic NCBI36 chr22: 17,008,132-20,213,879 , GRCh37.p13 chr22: 18,628,132-21,883,879 , GRCh38.p12 chr22: 18,145,365-21,529,590 ESS2, KLHL22, 146 more genes
    nsv3907554copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,626,108-21,800,797 , GRCh38.p12 chr22: 18,143,341-21,446,508 ESS2, RNY1P9, 144 more genes
    nsv4436810copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,631,364-21,800,471 , GRCh38.p12 chr22: 18,148,597-21,446,182 ESS2, FAM230E, 144 more genes
    nsv4436778copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,636,749-21,800,471 , GRCh38.p12 chr22: 18,153,982-21,446,182 ESS2, FAM247A, 144 more genes
    nsv6637364copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,644,543-21,800,797 , GRCh38.p12 chr22: 18,161,776-21,446,508 ESS2, LOC112268297, 144 more genes
    nsv3908988copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,644,790-21,800,471 , GRCh38.p12 chr22: 18,162,023-21,446,182 ESS2, CLTCL1, 144 more genes
    nsv6315533copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,645,353-21,800,797 , GRCh38.p12 chr22: 18,162,586-21,446,508 ESS2, GGT2P, 144 more genes
    nsv3909202copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,644,790-21,798,907 , GRCh38.p12 chr22: 18,162,023-21,444,618 ESS2, CA15P2, 144 more genes
    nsv3896759copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,648,866-21,800,797 , GRCh38.p12 chr22: 18,166,099-21,446,508 ESS2, MIR185, 144 more genes
    nsv3902067copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,648,866-21,798,907 , GRCh38.p12 chr22: 18,166,099-21,444,618 ESS2, LOC112268289, 144 more genes
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