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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2663569copy number variation1estd199human GRCh37 chr7: 110,872,001-110,963,909 , GRCh38.p12 chr7: 111,231,945-111,323,853 IMMP2L
    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
    esv2660522copy number variation236estd199human GRCh37 chr1: 207,700,012-207,737,123 , GRCh38.p12 chr1: 207,526,667-207,563,778 CR1
    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
    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
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2665445copy number variation9estd199human GRCh37 chr4: 120,332,945-120,352,176 , GRCh38.p12 chr4: 119,411,790-119,431,021
    esv2663734copy number variation40estd199human GRCh37 chr7: 5,936,562-5,951,173 , GRCh38.p12 chr7: 5,896,931-5,911,542 CCZ1
    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
    esv2678954copy number variation43estd199human GRCh37 chr3: 56,607,727-56,621,584 , GRCh38.p12 chr3: 56,573,699-56,587,556 CCDC66
    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
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    esv2665595copy number variation24estd199human GRCh37 chr18: 66,745,845-66,758,892 , GRCh38.p12 chr18: 69,078,608-69,091,655 CCDC102B
    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
    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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