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Items: 1 to 20 of 98

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946328copy number variation1nstd209human GRCh38 chr20: 3,914,036-3,915,542 , GRCh37.p13 chr20: 3,894,683-3,896,189 PANK2, MIR103A2, 1 more genes
    nsv5934392copy number variation1nstd209human GRCh38 chr20: 3,792,203-4,972,872 , GRCh37.p13 chr20: 3,772,850-4,953,518 FTLP3, PANK2-AS1, 23 more genes
    nsv5564166copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,190,178-3,903,961 , GRCh38.p12 chr20: 3,209,532-3,923,314 ADAM33, AP5S1, 23 more genes
    nsv5514711copy number variation1nstd206human GRCh38 chr20: 3,914,014-3,915,572 , GRCh37.p13 chr20: 3,894,661-3,896,219 MIR103A2, PANK2, 1 more genes
    nsv5033561inversion1nstd200human GRCh38 chr20: 3,693,712-5,966,244 , GRCh37.p13 chr20: 3,674,359-5,946,890 , LOC107985411, 53 more genes
    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
    nsv4457737copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,838,806-3,898,983 , GRCh38.p12 chr20: 3,858,159-3,918,336 PANK2, PANK2-AS1, 3 more genes
    nsv4457533copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,844,173-4,031,301 , GRCh38.p12 chr20: 3,863,526-4,050,654 MIR103A2, PANK2-AS1, 5 more genes
    nsv4457419copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,796,763-3,896,539 , GRCh38.p12 chr20: 3,816,116-3,915,892 AP5S1, PANK2-AS1, 4 more genes
    nsv4425349copy number variation1nstd174human GRCh37 chr20: 3,894,598-3,896,276 , GRCh38.p12 chr20: 3,913,951-3,915,629 PANK2, MIR103A2, 1 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
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