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Items: 1 to 20 of 102

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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
    nsv5329250copy number variation1nstd204human GRCh38.p13 chr20: 2,800,117-2,800,231 , GRCh37.p13 chr20: 2,780,763-2,780,877 CPXM1
    nsv5012175copy number variation1nstd200human GRCh38 chr20: 2,789,947-2,796,710 , GRCh37.p13 chr20: 2,770,593-2,777,356 CPXM1
    nsv4861661copy number variation1nstd200human GRCh37 chr20: 2,770,593-2,777,356 , GRCh38.p12 chr20: 2,789,947-2,796,710 CPXM1
    nsv4457667copy number variation1nstd102humanUncertain significance GRCh37 chr20: 2,738,670-3,054,217 , GRCh38.p12 chr20: 2,758,024-3,073,571 CPXM1, RPL19P1, 10 more genes
    nsv4422729copy number variation1nstd174human GRCh37 chr20: 2,631,269-2,970,332 , GRCh38.p12 chr20: 2,650,623-2,989,686 , VPS16, 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
    nsv3968363copy number variation1nstd168human GRCh38 chr20: 2,793,342-2,844,769 , GRCh37.p13 chr20: 2,773,988-2,825,415 VPS16, CPXM1, 3 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
    nsv3921981copy number variation1nstd102humanUncertain significance GRCh38 chr20: 2,595,077-3,004,837 , NCBI36 chr20: 2,523,723-2,933,483 , GRCh37 chr20: 2,575,723-2,985,483 IDH3B, TMEM239, 17 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
    nsv3920692copy number variation1nstd102humanUncertain significance GRCh37 chr20: 2,507,401-3,062,297 , NCBI36 chr20: 2,455,401-3,010,297 , GRCh38 chr20: 2,526,755-3,081,651 TMC2, MRPS26, 23 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
    nsv3914413copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-19,000,139 , GRCh38 chr20: 89,939-19,071,495 , GRCh37 chr20: 70,580-19,052,139 ZNF343, C20orf96, 331 more genes
    nsv3914070copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,928-18,688,031 , NCBI36 chr20: 9,569-18,616,675 , GRCh37 chr20: 61,569-18,668,675 CDC25B, LOC105372517, 324 more genes
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