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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5932105copy number variation1nstd209human GRCh38 chr20: 5,996,229-5,996,470 , GRCh37.p13 chr20: 5,976,875-5,977,116 MCM8, MCM8-AS1
    nsv5522498copy number variation1nstd206human GRCh38 chr20: 6,000,583-6,000,660 , GRCh37.p13 chr20: 5,981,229-5,981,306 MCM8, RN7SL498P, 1 more genes
    nsv4558681insertion1nstd166human GRCh37.p13 chr20: 5,976,596-5,976,596 , GRCh38.p12 chr20: 5,995,950-5,995,950 MCM8-AS1, MCM8
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 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
    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
    nsv3918185copy number variation1nstd102humanUncertain significance NCBI36 chr20: 5,873,572-6,048,235 , GRCh37.p13 chr20: 5,925,572-6,100,235 , GRCh38.p12 chr20: 5,944,926-6,119,588 RN7SL498P, LRRN4, 5 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
    nsv3913796copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-28,133,653 , GRCh37.p13 chr20: 70,580-29,519,992 , GRCh38.p12 chr20: 89,939-30,285,316 RNY4P11, EIF4E2P1, 500 more genes
    nsv3913704copy number variation1nstd102humanPathogenic GRCh38 chr20: 89,939-25,697,564 , NCBI36 chr20: 18,580-25,626,200 , GRCh37 chr20: 70,580-25,678,200 NRSN2, LOC102724545, 459 more genes
    nsv3913573copy number variation1nstd102humanPathogenic GRCh38 chr20: 1,269,303-8,626,911 , NCBI36 chr20: 1,197,947-8,555,558 , GRCh37 chr20: 1,249,947-8,607,558 LINC01433, NOP56, 158 more genes
    nsv3913207copy number variation1nstd102humanPathogenic GRCh38 chr20: 4,343,033-6,911,730 , GRCh37 chr20: 4,323,680-6,892,377 , NCBI36 chr20: 4,271,680-6,840,377 RNA5-8SP7, PRNP, 45 more genes
    nsv3912889copy number variation1nstd102humanPathogenic NCBI36 chr20: 8,734-6,314,659 , GRCh37 chr20: 60,734-6,366,659 , GRCh38 chr20: 80,093-6,386,012 IDH3B, NOP56, 172 more genes
    nsv3908959copy number variation1nstd102humanPathogenic GRCh37 chr20: 67,837-29,638,363 , GRCh38.p12 chr20: 87,196-30,403,687 ISM1-AS1, CST9LP2, 504 more genes
    nsv3907558copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-26,075,841 , GRCh38.p12 chr20: 99,557-26,095,205 LINC03086, RN7SKP69, 469 more genes
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