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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5932813copy number variation1nstd209human GRCh38 chr20: 3,820,938-3,844,143 , GRCh37.p13 chr20: 3,801,585-3,824,790 AP5S1
    nsv5886983copy number variation1nstd209human GRCh38 chr20: 3,820,725-3,828,582 , GRCh37.p13 chr20: 3,801,372-3,809,229 AP5S1
    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
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5516183copy number variation1nstd206human GRCh38 chr20: 3,820,732-3,820,812 , GRCh37.p13 chr20: 3,801,379-3,801,459 AP5S1
    nsv5514495copy number variation1nstd206human GRCh38 chr20: 3,814,700-3,827,435 , GRCh37.p13 chr20: 3,795,347-3,808,082 AP5S1
    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
    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
    nsv4428901copy number variation1nstd174human GRCh37 chr20: 3,794,868-3,799,230 , GRCh38.p12 chr20: 3,814,221-3,818,583 AP5S1
    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
    nsv4252975copy number variation1nstd166human GRCh37.p13 chr20: 3,801,542-3,824,819 , GRCh38.p12 chr20: 3,820,895-3,844,172 AP5S1
    nsv3956825copy number variation1nstd168human GRCh38 chr20: 3,822,901-3,857,464 , GRCh37.p13 chr20: 3,803,548-3,838,111 MAVS, AP5S1
    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
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