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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962086copy number variation1nstd209human GRCh38 chr20: 32,122,552-32,122,630 , GRCh37.p13 chr20: 30,710,355-30,710,433 TM9SF4
    nsv5702423mobile element insertion1nstd211human GRCh38 chr20: 32,145,598-32,145,598 , GRCh37.p13 chr20: 30,733,401-30,733,401 TM9SF4
    nsv5670918insertion1nstd207human GRCh38 chr20: 32,123,203-32,123,203 , GRCh37.p13 chr20: 30,711,006-30,711,006 TM9SF4
    nsv5587540copy number variation1nstd207human GRCh38 chr20: 32,122,010-32,122,186 , GRCh37.p13 chr20: 30,709,813-30,709,989 TM9SF4
    nsv5550216insertion1nstd206human GRCh38 chr20: 32,147,161-32,147,181 , GRCh37.p13 chr20: 30,734,964-30,734,984 TM9SF4
    nsv5422745mobile element insertion1nstd206human GRCh38 chr20: 32,145,598-32,145,649 , GRCh37.p13 chr20: 30,733,401-30,733,452 TM9SF4
    nsv5350289translocation1nstd200human GRCh38 chr20: 32,159,335-32,159,335 , GRCh38 chr20: 32,159,417-32,159,417 , GRCh37.p13 chr20: 30,747,220-30,747,220 , GRCh37.p13 chr20: 30,747,138-30,747,138 , TM9SF4
    nsv5283549copy number variation1nstd204human GRCh38.p13 chr20: 31,227,801-32,548,400 , GRCh37.p13 chr20: 29,815,604-31,136,202 , XKR7, 52 more genes
    nsv5172180mobile element insertion1nstd203human GRCh38 chr20: 32,128,222-32,128,236 , GRCh37.p13 chr20: 30,716,025-30,716,039 TM9SF4
    nsv5166050mobile element insertion1nstd203human GRCh38 chr20: 32,138,311-32,138,324 , GRCh37.p13 chr20: 30,726,114-30,726,127 TM9SF4
    nsv5022325copy number variation1nstd200human GRCh38 chr20: 32,134,858-32,137,250 , GRCh37.p13 chr20: 30,722,661-30,725,053 TM9SF4
    nsv4868577copy number variation1nstd200human GRCh37 chr20: 30,722,661-30,725,053 , GRCh38.p12 chr20: 32,134,858-32,137,250 TM9SF4
    nsv4736678copy number variation1nstd199human GRCh37 chr20: 30,710,059-30,710,110 , GRCh38.p12 chr20: 32,122,256-32,122,307 TM9SF4
    nsv4509474mobile element insertion1nstd166human GRCh37.p13 chr20: 30,726,114-30,726,114 , GRCh38.p12 chr20: 32,138,311-32,138,311 TM9SF4
    nsv4500542mobile element insertion1nstd166human GRCh37.p13 chr20: 30,733,386-30,733,386 , GRCh38.p12 chr20: 32,145,583-32,145,583 TM9SF4
    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
    nsv3956330copy number variation1nstd168human GRCh38 chr20: 32,158,496-32,167,442 , GRCh37.p13 chr20: 30,746,299-30,755,245 , TM9SF4
    nsv3930787copy number variation1nstd167human GRCh37 chr20: 30,710,014-30,710,062 , GRCh38.p12 chr20: 32,122,211-32,122,259 TM9SF4
    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
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