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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4861822copy number variation1nstd200human GRCh37 chr20: 6,748,523-6,748,607 , GRCh38.p12 chr20: 6,767,876-6,767,960 LOC105372517, BMP2
    nsv4682046copy number variation1nstd102humanPathogenic GRCh37 chr20: 6,015,110-6,759,736 , GRCh38.p12 chr20: 6,034,464-6,779,089 CASC20, TARDBPP1, 8 more genes
    nsv4567566insertion1nstd166human GRCh37.p13 chr20: 6,751,232-6,751,232 , GRCh38.p12 chr20: 6,770,585-6,770,585 BMP2
    nsv4566492sequence alteration1nstd166human GRCh37.p13 chr20: 6,738,001-6,754,593 , GRCh38.p12 chr20: 6,757,354-6,773,946 BMP2, LOC105372517
    nsv4502117mobile element insertion1nstd166human GRCh37.p13 chr20: 6,758,139-6,758,139 , GRCh38.p12 chr20: 6,777,492-6,777,492 BMP2
    nsv4457637copy number variation1nstd102humanUncertain significance GRCh37 chr20: 6,237,506-7,074,125 , GRCh38.p12 chr20: 6,256,859-7,093,478 LINC01713, BMP2, 2 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
    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
    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
    nsv3915947copy number variation1nstd102humanPathogenic GRCh38 chr20: 6,336,607-8,577,546 , NCBI36 chr20: 6,265,254-8,506,193 , GRCh37 chr20: 6,317,254-8,558,193 TMX4, HAO1, 15 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
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