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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5280921copy number variation1nstd204human GRCh38.p13 chr20: 3,151,601-3,155,800 , GRCh37.p13 chr20: 3,132,247-3,136,446 UBOX5, FASTKD5
    nsv5168576mobile element insertion1nstd203human GRCh38 chr20: 3,146,410-3,146,425 , GRCh37.p13 chr20: 3,127,056-3,127,071 UBOX5, FASTKD5, 1 more genes
    nsv4861683copy number variation1nstd200human GRCh37 chr20: 3,138,905-3,139,373 , GRCh38.p12 chr20: 3,158,259-3,158,727 UBOX5, FASTKD5
    nsv4729952copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,116,478-4,199,486 , GRCh38.p12 chr20: 3,135,832-4,218,839 LOC105372508, CDC25B, 35 more genes
    nsv4729947copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,092,739-4,939,933 , GRCh38.p12 chr20: 3,112,093-4,959,287 SF3A3P1, PRND, 46 more genes
    nsv4729753copy number variation1nstd102humanUncertain significance GRCh37 chr20: 2,802,218-4,010,802 , GRCh38.p12 chr20: 2,821,572-4,030,155 DDRGK1, LZTS3, 40 more genes
    nsv4676134copy number variation1nstd102humanUncertain significance GRCh37 chr20: 2,806,498-4,007,381 , GRCh38.p12 chr20: 2,825,852-4,026,734 MIR103B2, OXT, 40 more genes
    nsv4626453copy number variation1nstd183human GRCh37 chr20: 3,020,553-3,350,814 , GRCh38.p12 chr20: 3,039,907-3,370,167 DDRGK1, FASTKD5, 16 more genes
    nsv4535422copy number variation1nstd166human GRCh37.p13 chr20: 3,136,738-3,139,722 , GRCh38.p12 chr20: 3,156,092-3,159,076 UBOX5, FASTKD5
    nsv4417768copy number variation1nstd174human GRCh37 chr20: 3,011,188-3,385,073 , GRCh38.p12 chr20: 3,030,542-3,404,426 LZTS3, UBOX5, 17 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
    nsv4330625inversion1nstd166human GRCh37.p13 chr20: 2,496,151-5,491,306 , GRCh38.p12 chr20: 2,515,505-5,510,660 , ADRA1D, 89 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
    nsv3922038copy number variation1nstd102humanUncertain significance GRCh38 chr20: 80,927-5,447,679 , NCBI36 chr20: 9,568-5,376,325 , GRCh37 chr20: 61,568-5,428,325 LOC105372509, SIRPD, 150 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
    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
    nsv3919009copy number variation1nstd102humanPathogenic NCBI36 chr20: 13,043-6,087,725 , GRCh37 chr20: 65,043-6,139,725 , GRCh38 chr20: 84,402-6,159,078 PCED1A, TBC1D20, 169 more genes
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