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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3884386copy number variation1nstd102humanBenign GRCh37 chr2: 228,637,113-228,685,262 , GRCh38.p12 chr2: 227,772,397-227,820,546 CCL20, SNRPGP8, 1 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 CCL20, DAZAP2P1, 2991 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 CCL20, LOC105373947, 357 more genes
    nsv3893827copy number variation1nstd102humanPathogenic NCBI36 chr2: 227,551,089-237,459,981 , GRCh38 chr2: 226,978,129-236,886,599 , GRCh37 chr2: 227,842,845-237,795,242 CCL20, B3GNT7, 193 more genes
    nsv3881953copy number variation1nstd102humanPathogenic GRCh37 chr2: 223,378,640-232,061,074 , GRCh38.p12 chr2: 222,513,921-231,196,360 CCL20, LOC105373925, 112 more genes
    nsv3906029copy number variation1nstd102humanPathogenic NCBI36 chr2: 227,916,238-235,912,551 , GRCh38 chr2: 227,343,278-235,339,168 , GRCh37 chr2: 228,207,994-236,247,812 CCL20, SP110, 167 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 CCL20, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 CCL20, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 CCL20, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 CCL20, MTND2P22, 3724 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 CCL20, LOC105376755, 1013 more genes
    nsv3890898copy number variation1nstd102humanPathogenic GRCh38 chr2: 188,818,195-242,065,208 , NCBI36 chr2: 189,391,166-242,656,032 , GRCh37 chr2: 189,682,921-243,007,359 CCL20, LOC105373909, 901 more genes
    nsv3896499copy number variation1nstd102humanPathogenic GRCh37 chr2: 190,300,875-242,783,384 , NCBI36 chr2: 190,009,120-242,432,057 , GRCh38 chr2: 189,436,149-241,841,232 CCL20, RNU6-1206P, 883 more genes
    nsv3908112copy number variation1nstd102humanPathogenic GRCh38 chr2: 190,310,736-241,892,770 , NCBI36 chr2: 190,883,707-242,483,594 , GRCh37 chr2: 191,175,462-242,834,921 CCL20, LOC101928084, 871 more genes
    nsv3892046copy number variation1nstd102humanPathogenic GRCh37 chr2: 195,763,507-237,382,556 , NCBI36 chr2: 195,471,752-237,047,295 , GRCh38 chr2: 194,898,783-236,473,913 CCL20, NPM1P46, 706 more genes
    nsv3892823copy number variation1nstd102humanPathogenic GRCh37 chr2: 211,444,400-243,059,659 , GRCh38 chr2: 210,579,676-242,126,245 , NCBI36 chr2: 211,152,645-242,717,069 CCL20, RPL19P5, 567 more genes
    nsv3871121copy number variation1nstd102humanPathogenic GRCh37 chr2: 213,518,431-242,783,384 , GRCh38.p12 chr2: 212,653,707-241,841,232 CCL20, TWIST2, 544 more genes
    nsv4435891copy number variation1nstd102humanPathogenic GRCh37 chr2: 210,779,657-239,879,183 , GRCh38.p12 chr2: 209,914,933-238,957,487 CCL20, XRCC5, 494 more genes
    nsv3894025copy number variation1nstd102humanPathogenic NCBI36 chr2: 218,674,727-242,717,069 , GRCh37 chr2: 218,966,482-243,059,659 , GRCh38 chr2: 218,101,759-242,126,245 CCL20, DNAJB6P3, 483 more genes
    nsv3884002copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,225,872-242,016,876 , GRCh38.p12 chr2: 218,361,149-241,077,461 CCL20, LOC107985990, 428 more genes
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