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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2662218copy number variation44estd199human GRCh37 chr7: 52,171,112-52,397,355 , GRCh38.p12 chr7: 52,103,416-52,329,659 LOC107986796
    esv2667872copy number variation147estd199human GRCh37 chr1: 225,133,630-225,248,654 , GRCh38.p12 chr1: 224,945,928-225,060,952 DNAH14
    esv2660370copy number variation2estd199human GRCh37 chr15: 94,149,998-94,243,725 , GRCh38.p12 chr15: 93,606,769-93,700,496 LOC107983974
    esv2676574copy number variation189estd199human GRCh37 chr6: 78,967,194-79,036,497 , GRCh38.p12 chr6: 78,257,477-78,326,780 LOC105377865
    esv2668226copy number variation311estd199human GRCh37 chr3: 129,763,245-129,799,692 , GRCh38.p12 chr3: 130,044,402-130,080,849 ALG1L2
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2676662copy number variation263estd199human GRCh37 chr19: 41,360,712-41,392,496 , GRCh38.p12 chr19: 40,854,807-40,886,591 CYP2A7
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2667383copy number variation138estd199human GRCh37 chr2: 98,139,645-98,158,592 , GRCh38.p12 chr2: 97,523,182-97,542,129 ANKRD36B
    esv2663133copy number variation46estd199human GRCh37 chr6: 32,629,745-32,648,392 , GRCh38.p12 chr6: 32,661,968-32,680,615 HLA-DQB1
    esv2674493copy number variation111estd199human GRCh37 chr1: 169,225,645-169,243,192 , GRCh38.p12 chr1: 169,256,407-169,273,954 NME7
    esv2674647copy number variation204estd199human GRCh37 chr8: 56,377,729-56,393,641 , GRCh38.p12 chr8: 55,465,169-55,481,081 XKR4
    esv2669960copy number variation208estd199human GRCh37 chr9: 41,968,745-41,984,492 , GRCh38.p12 chr9: 39,823,727-39,839,474 FGF7P3
    esv2670787copy number variation158estd199human GRCh37 chr7: 151,134-160,557 , GRCh38.p12 chr7: 151,134-160,557 , GRCh38.p12 chr7|NT_187558.1: 106,939-119,904 , GRCh38.p12 chr7|NT_187653.1: 143,455-152,878 LINC03014
    esv2664803copy number variation436estd199human GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597 SCAPER
    esv2678677copy number variation179estd199human GRCh37 chr15: 76,884,295-76,895,742 , GRCh38.p12 chr15: 76,591,954-76,603,401 SCAPER
    esv2677965copy number variation40estd199human GRCh37 chr4: 92,073,713-92,084,451 , GRCh38.p12 chr4: 91,152,562-91,163,300 CCSER1
    esv2674062copy number variation28estd199human GRCh37 chr7: 89,519,904-89,530,436 , GRCh38.p12 chr7: 89,890,590-89,901,122 STEAP2-AS1
    esv2678726copy number variation12estd199human GRCh37 chr14: 47,707,571-47,717,845 , GRCh38.p12 chr14: 47,238,368-47,248,642 MDGA2
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