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Items: 1 to 20 of 1782

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2676068copy number variation152estd199human GRCh37 chr6: 32,454,245-32,511,792 , GRCh38.p12 chr6: 32,486,468-32,544,015 HLA-DRB5
    esv2664200copy number variation92estd199human GRCh37 chr4: 75,282,645-75,323,192 , GRCh38.p12 chr4: 74,416,928-74,457,475 AREG
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2666578copy number variation167estd199human GRCh37 chr17: 77,462,245-77,494,392 , GRCh38.p12 chr17: 79,466,163-79,498,310 RBFOX3
    esv2676662copy number variation263estd199human GRCh37 chr19: 41,360,712-41,392,496 , GRCh38.p12 chr19: 40,854,807-40,886,591 CYP2A7
    esv2658850copy number variation59estd199human GRCh37 chr16: 55,794,745-55,822,692 , GRCh38.p12 chr16: 55,760,833-55,788,780 CES1P1
    esv2661219copy number variation458estd199human GRCh37 chr8: 48,180,445-48,214,692 , GRCh38.p12 chr8: 47,276,396-47,302,103 SPIDR
    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
    esv2675464copy number variation4estd199human GRCh37 chr16: 12,412,525-12,430,086 , GRCh38.p12 chr16: 12,318,668-12,336,229 SNX29
    esv2672929copy number variation23estd199human GRCh37 chr16: 60,081,112-60,098,561 , GRCh38.p12 chr16: 60,047,208-60,064,657 LINC02141
    esv2662901copy number variation324estd199human GRCh37 chr9: 41,969,445-41,984,392 , GRCh38.p12 chr9: 39,824,427-39,839,374 FGF7P3
    esv2663734copy number variation40estd199human GRCh37 chr7: 5,936,562-5,951,173 , GRCh38.p12 chr7: 5,896,931-5,911,542 CCZ1
    esv2662537copy number variation71estd199human GRCh37 chr3: 75,567,345-75,581,692 , GRCh38.p12 chr3: 75,518,194-75,532,541 SNRPCP10
    esv2661760copy number variation42estd199human GRCh37 chr7: 62,965,045-62,979,392 , GRCh38.p12 chr7: 63,504,667-63,519,014 PHKG1P2
    esv2668407copy number variation98estd199human GRCh37 chr11: 55,445,645-55,459,892 , GRCh38.p12 chr11: 55,678,169-55,692,416 OR4P1P
    esv2675982copy number variation92estd199human GRCh37 chr8: 21,624,845-21,638,692 , GRCh38.p12 chr8: 21,767,333-21,781,180 GFRA2
    esv2666505copy number variation53estd199human GRCh37 chr3: 195,457,318-195,471,074 , GRCh38.p12 chr3|NT_187678.1: 51,829-65,597 , GRCh38.p12 chr3|NT_187688.1: 50,529-64,252 , GRCh38.p12 chr3|NT_187689.1: 100,944-114,700 , GRCh38.p12 chr3|NT_187690.1: 50,528-64,259 , GRCh38.p12 chr3|NT_187691.1: 50,635-64,429 , GRCh38.p12 chr3|NT_187532.1: 100,944-114,700 , GRCh38.p12 chr3|NT_187649.1: 50,533-64,252 , GRCh38.p12 chr3: 195,730,447-195,744,203 MUC20
    esv2665595copy number variation24estd199human GRCh37 chr18: 66,745,845-66,758,892 , GRCh38.p12 chr18: 69,078,608-69,091,655 CCDC102B
    esv2669985copy number variation97estd199human GRCh37 chr19: 1,852,045-1,864,992 , GRCh38.p12 chr19: 1,852,046-1,864,993 KLF16
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