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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5948413copy number variation1nstd209human GRCh38 chr20: 35,671,536-35,737,524 , GRCh37.p13 chr20: 34,259,458-34,325,446 NFS1, RBM39, 1 more genes
    nsv5874371copy number variation2nstd209human GRCh38 chr20: 35,696,762-35,697,861 , GRCh37.p13 chr20: 34,284,684-34,285,783 NFS1, ROMO1
    nsv5874203copy number variation1nstd209human GRCh38 chr20: 35,686,809-35,706,611 , GRCh37.p13 chr20: 34,274,731-34,294,533 NFS1, RBM39, 1 more genes
    nsv5708097mobile element insertion1nstd211human GRCh38 chr20: 35,697,489-35,697,489 , GRCh37.p13 chr20: 34,285,411-34,285,411 NFS1, ROMO1
    nsv5557509sequence alteration1nstd206human GRCh38 chr20: 35,627,992-36,077,048 , GRCh37.p13 chr20: 34,215,914-34,664,970 CPNE1, PHF20, 16 more genes
    nsv5432040mobile element insertion1nstd206human GRCh38 chr20: 35,697,489-35,697,540 , GRCh37.p13 chr20: 34,285,411-34,285,462 ROMO1, NFS1
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5022326copy number variation1nstd200human GRCh38 chr20: 32,216,214-44,981,731 , GRCh37.p13 chr20: 30,804,017-43,610,372 , HNF4A, 279 more genes
    nsv4868593copy number variation1nstd200human GRCh37 chr20: 31,164,049-45,167,425 , GRCh38.p12 chr20: 32,576,247-46,538,786 , MMP24-AS1-EDEM2, 350 more genes
    nsv4868578copy number variation1nstd200human GRCh37 chr20: 30,804,017-43,610,372 , GRCh38.p12 chr20: 32,216,214-44,981,731 , SNORA71C, 279 more genes
    nsv4457806copy number variation1nstd102humanPathogenic GRCh37 chr20: 29,833,608-35,087,952 , GRCh38.p12 chr20: 31,245,805-36,459,549 EFCAB8, C20orf203, 162 more genes
    nsv3968917insertion1nstd168human GRCh38 chr20: 35,696,547-35,699,737 , GRCh37.p13 chr20: 34,284,469-34,287,659 NFS1, RBM39, 1 more genes
    nsv3920503copy number variation1nstd102humanPathogenic GRCh38 chr20: 32,062,768-35,906,606 , NCBI36 chr20: 30,114,232-33,957,942 , GRCh37 chr20: 30,650,571-34,494,528 UQCC1, MIR1289-1, 111 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3918053copy number variation1nstd102humanPathogenic NCBI36 chr20: 25,703,100-38,491,480 , GRCh37.p13 chr20: 25,755,100-39,058,066 , GRCh38.p12 chr20: 25,774,464-40,429,426 MYH7B, PPP1R16B, 300 more genes
    nsv3913594copy number variation1nstd102humanPathogenic GRCh37 chr20: 32,020,169-35,450,284 , NCBI36 chr20: 31,483,830-34,883,698 , GRCh38 chr20: 33,432,363-36,821,881 AHCY, RALY, 93 more genes
    nsv3912723copy number variation1nstd102humanPathogenic NCBI36 chr20: 30,288,202-45,731,170 , GRCh37.p13 chr20: 30,824,541-46,297,763 , GRCh38.p12 chr20: 32,236,738-47,669,019 LOC107985448, LOC105372613, 370 more genes
    nsv3910818copy number variation1nstd102humanUncertain significance NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167 RNA5SP481, LOC105372625, 855 more genes
    nsv3910160copy number variation1nstd102humanPathogenic NCBI36 chr20: 33,336,941-33,796,173 , GRCh38 chr20: 35,285,724-35,744,837 , GRCh37 chr20: 33,873,527-34,332,759 CPNE1, ROMO1, 19 more genes
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