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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
    nsv5196877mobile element insertion1nstd203human GRCh38 chr20: 1,208,240-1,208,256 , GRCh37.p13 chr20: 1,188,884-1,188,900 C20orf202
    nsv4676288copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-1,305,971 , GRCh38.p12 chr20: 80,927-1,325,327 TBC1D20, RAD21L1, 34 more genes
    nsv4676270copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-2,269,777 , GRCh38.p12 chr20: 80,927-2,289,131 LOC100289473, STK35, 60 more genes
    nsv4676163copy number variation1nstd102humanUncertain significance GRCh37 chr20: 989,820-1,216,980 , GRCh38.p12 chr20: 1,009,177-1,236,336 C20orf202, PSMF1, 4 more genes
    nsv4457692copy number variation1nstd102humanUncertain significance GRCh37 chr20: 728,577-1,237,670 , GRCh38.p12 chr20: 747,933-1,257,026 TMEM74B, RAD21L1, 10 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
    nsv4268853copy number variation1nstd166human GRCh37.p13 chr20: 748,902-1,301,892 , GRCh38.p12 chr20: 768,258-1,321,248 , RAD21L1, 15 more genes
    nsv3924759copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-1,422,759 , GRCh38 chr20: 89,939-1,494,113 , GRCh37 chr20: 70,580-1,474,759 DEFB127, CSNK2A1, 39 more genes
    nsv3923563copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-1,699,213 , GRCh37 chr20: 70,580-1,751,213 , GRCh38 chr20: 89,939-1,770,567 LOC101929937, DEFB132, 50 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
    nsv3922564copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 8,747-1,175,535 , GRCh37 chr20: 60,747-1,227,535 , GRCh38 chr20: 80,106-1,246,891 ACTG1P3, CSNK2A1, 30 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
    nsv3921973copy number variation1nstd102humanUncertain significance GRCh37 chr20: 809,607-1,221,836 , GRCh38 chr20: 828,964-1,241,192 , NCBI36 chr20: 757,607-1,169,836 ACTG1P3, RAD21L1, 9 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
    nsv3917810copy number variation1nstd102humanPathogenic GRCh38 chr20: 121,781-2,290,194 , GRCh37 chr20: 102,422-2,270,840 , NCBI36 chr20: 50,422-2,218,840 RAD21L1, SIRPG-AS1, 59 more genes
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