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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381139copy number variation1nstd102humanUncertain significance GRCh37 chr20: 10,579,323-11,009,878 , GRCh38.p12 chr20: 10,598,675-11,029,230 LOC107985398, MIR6870, 7 more genes
    nsv5294962copy number variation1nstd204human GRCh38.p13 chr20: 10,669,401-10,673,200 , GRCh37.p13 chr20: 10,650,049-10,653,848 JAG1
    nsv5174624mobile element insertion1nstd203human GRCh38 chr20: 10,669,547-10,669,588 , GRCh37.p13 chr20: 10,650,195-10,650,236 JAG1
    nsv5166960mobile element insertion1nstd203human GRCh38 chr20: 10,670,530-10,670,545 , GRCh37.p13 chr20: 10,651,178-10,651,193 JAG1
    nsv4861926copy number variation1nstd200human GRCh37 chr20: 10,628,838-10,628,904 , GRCh38.p12 chr20: 10,648,190-10,648,256 MIR6870, JAG1
    nsv4676419copy number variation1nstd102humanPathogenic GRCh37 chr20: 8,571,696-22,088,650 , GRCh38.p12 chr20: 8,591,049-22,108,012 PGAM3P, EEF1A1P34, 182 more genes
    nsv4565435sequence alteration1nstd166human GRCh37.p13 chr20: 10,627,264-10,627,265 , GRCh38.p12 chr20: 10,646,616-10,646,617 JAG1
    nsv4511868mobile element insertion1nstd166human GRCh37.p13 chr20: 10,651,178-10,651,178 , GRCh38.p12 chr20: 10,670,530-10,670,530 JAG1
    nsv4510840mobile element insertion1nstd166human GRCh37.p13 chr20: 10,624,847-10,624,847 , GRCh38.p12 chr20: 10,644,199-10,644,199 JAG1
    nsv4449772copy number variation1nstd102humanPathogenic GRCh37 chr20: 10,234,257-10,654,198 , GRCh38 chr20: 10,253,609-10,673,550 JAG1, SNAP25, 7 more genes
    nsv4349454copy number variation1nstd102humanPathogenic GRCh37 chr20: 10,124,855-11,479,105 , GRCh38.p12 chr20: 10,144,207-11,498,457 SNAP25, LOC100421490, 19 more genes
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
    nsv4336704sequence alteration1nstd166human GRCh37.p13 chr20: 8,105,854-23,795,733 , GRCh38.p12 chr20: 8,125,207-23,815,096 , BFSP1, 242 more genes
    nsv3923490copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-13,029,401 , NCBI36 chr20: 8,747-12,958,049 , GRCh37 chr20: 60,747-13,010,049 LINC01751, RNA5SP474, 238 more genes
    nsv3922272copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-30,227,427 , NCBI36 chr20: 8,747-28,075,764 , GRCh37 chr20: 60,747-29,462,103 ISM1-AS1, CST2, 498 more genes
    nsv3922170copy number variation1nstd102humanPathogenic NCBI36 chr20: 9,479,622-12,012,082 , GRCh38 chr20: 9,550,975-12,083,434 , GRCh37 chr20: 9,531,622-12,064,082 LOC107985384, PGAM3P, 32 more genes
    nsv3921972copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-19,074,923 , GRCh38 chr20: 89,939-19,146,279 , GRCh37 chr20: 70,580-19,126,923 PTMAP3, LOC105372517, 331 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
    nsv3920089copy number variation1nstd102humanPathogenic GRCh38 chr20: 6,617,695-13,392,559 , NCBI36 chr20: 6,546,342-13,321,206 , GRCh37 chr20: 6,598,342-13,373,206 RN7SKP111, LOC105372517, 68 more genes
    nsv3919898copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38 chr20: 80,927-26,324,843 , NCBI36 chr20: 9,568-26,253,479 MIR3192, CFAP61, 473 more genes
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