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Items: 1 to 20 of 416

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144227copy number variation1nstd232human GRCh37.p13 chr1: 155,698,911-155,698,995 , GRCh38.p12 chr1: 155,729,120-155,729,204 DAP3
    nsv7138507insertion1nstd232human GRCh37.p13 chr1: 155,697,528-155,697,528 , GRCh38.p12 chr1: 155,727,737-155,727,737 DAP3
    nsv7099235copy number variation1nstd231human GRCh38.p12 chr1: 154,116,919-155,715,830 , GRCh37 chr1: 154,089,395-155,685,621 ADAR, CHRNB2, 80 more genes
    nsv7095755copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr1: 155,581,953-155,880,552 , GRCh38.p12 chr1: 155,612,162-155,910,761 SYT11, RIT1, 12 more genes
    nsv7057328inversion1nstd229human GRCh38 chr1: 154,938,555-155,849,490 , GRCh37.p13 chr1: 154,911,031-155,819,281 ENTREP3, YY1AP1, 57 more genes
    nsv7056666inversion1nstd229human GRCh38 chr1: 151,403,323-155,722,147 , GRCh37.p13 chr1: 151,375,799-155,691,938 ILF2, SPRR2C, 219 more genes
    nsv7055468inversion1nstd229human GRCh38 chr1: 155,667,181-158,101,472 , GRCh37.p13 chr1: 155,636,972-158,071,262 FCRL4, CRABP2, 88 more genes
    nsv7041047inversion1nstd229human GRCh38 chr1: 154,596,558-159,585,927 , GRCh37.p13 chr1: 154,569,034-159,555,717 ADAR, SNORA80E, 204 more genes
    nsv7039558inversion1nstd229human GRCh38 chr1: 155,298,171-158,468,090 , GRCh37.p13 chr1: 155,267,962-158,437,880 FCRL4, SCARNA4, 121 more genes
    nsv6642735copy number variation1nstd229human GRCh38 chr1: 155,689,968-155,694,674 , GRCh37.p13 chr1: 155,659,759-155,664,465 DAP3
    nsv6642516copy number variation1nstd229human GRCh38 chr1: 155,726,842-155,727,528 , GRCh37.p13 chr1: 155,696,633-155,697,319 DAP3
    nsv6642515copy number variation1nstd229human GRCh38 chr1: 155,719,169-155,719,453 , GRCh37.p13 chr1: 155,688,960-155,689,244 DAP3
    nsv6642511copy number variation1nstd229human GRCh38 chr1: 155,605,388-155,743,015 , GRCh37.p13 chr1: 155,575,179-155,712,806 YY1AP1, LOC100419799, 5 more genes
    nsv6642386copy number variation1nstd229human GRCh38 chr1: 155,688,901-155,694,800 , GRCh37.p13 chr1: 155,658,692-155,664,591 YY1AP1, DAP3
    nsv6642385copy number variation1nstd229human GRCh38 chr1: 155,688,301-155,693,800 , GRCh37.p13 chr1: 155,658,092-155,663,591 DAP3, YY1AP1
    nsv6642376copy number variation1nstd229human GRCh38 chr1: 155,519,942-155,828,116 , GRCh37.p13 chr1: 155,489,733-155,797,907 LOC100505728, DAP3P1, 14 more genes
    nsv6642281copy number variation1nstd229human GRCh38 chr1: 155,718,172-155,719,917 , GRCh37.p13 chr1: 155,687,963-155,689,708 DAP3
    nsv6642280copy number variation1nstd229human GRCh38 chr1: 155,715,419-155,721,706 , GRCh37.p13 chr1: 155,685,210-155,691,497 DAP3
    nsv6642270copy number variation1nstd229human GRCh38 chr1: 155,417,134-155,818,120 , GRCh37.p13 chr1: 155,386,925-155,787,911 LOC100419798, RNU6-1297P, 16 more genes
    nsv6637136copy number variation1nstd102humanUncertain significance GRCh37 chr1: 155,489,474-156,196,407 , GRCh38.p12 chr1: 155,519,683-156,226,616 YY1AP1, ASH1L, 37 more genes
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