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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
    esv2674484copy number variation82estd199human GRCh37 chr1: 225,133,646-225,248,670 , GRCh38.p12 chr1: 224,945,944-225,060,968 DNAH14
    esv2676574copy number variation189estd199human GRCh37 chr6: 78,967,194-79,036,497 , GRCh38.p12 chr6: 78,257,477-78,326,780 LOC105377865
    esv2670203copy number variation158estd199human GRCh37 chr6: 78,967,194-79,036,475 , GRCh38.p12 chr6: 78,257,477-78,326,758 LOC105377865
    esv2678472copy number variation114estd199human GRCh37 chr14: 41,609,436-41,669,664 , GRCh38.p12 chr14: 41,140,233-41,200,461 LINC02315
    esv2676068copy number variation152estd199human GRCh37 chr6: 32,454,245-32,511,792 , GRCh38.p12 chr6: 32,486,468-32,544,015 HLA-DRB5
    esv2672105copy number variation71estd199human GRCh37 chr20: 1,553,045-1,594,292 , GRCh38.p12 chr20: 1,572,399-1,613,646 SIRPB1
    esv2676981copy number variation78estd199human GRCh37 chr19: 41,345,203-41,375,827 , GRCh38.p12 chr19: 40,839,298-40,869,922 CYP2A6
    esv2663419copy number variation22estd199human GRCh37 chr4: 8,976,940-9,000,688 , GRCh38.p12 chr4: 8,975,214-8,998,962 OR7E111FP
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2660999copy number variation147estd199human GRCh37 chr1: 169,224,745-169,246,292 , GRCh38.p12 chr1: 169,255,507-169,277,054 NME7
    esv2674235copy number variation67estd199human GRCh37 chr2: 98,139,745-98,158,992 , GRCh38.p12 chr2: 97,523,282-97,542,529 ANKRD36B
    esv2669960copy number variation208estd199human GRCh37 chr9: 41,968,745-41,984,492 , GRCh38.p12 chr9: 39,823,727-39,839,474 FGF7P3
    esv2659061copy number variation59estd199human GRCh37 chr7: 100,327,245-100,342,892 , GRCh38.p12 chr7: 100,729,622-100,745,269 ZAN
    esv2670832copy number variation47estd199human GRCh37 chr3: 195,457,248-195,471,004 , GRCh38.p12 chr3|NT_187688.1: 50,599-64,322 , GRCh38.p12 chr3|NT_187689.1: 100,874-114,630 , GRCh38.p12 chr3|NT_187690.1: 50,598-64,329 , GRCh38.p12 chr3|NT_187691.1: 50,705-64,499 , GRCh38.p12 chr3|NT_187532.1: 100,874-114,630 , GRCh38.p12 chr3|NT_187649.1: 50,603-64,322 , GRCh38.p12 chr3: 195,730,377-195,744,133 , GRCh38.p12 chr3|NT_187678.1: 51,899-65,667 MUC20
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    esv2656701copy number variation437estd199human GRCh37 chr16: 78,371,638-78,384,898 , GRCh38.p12 chr16: 78,337,741-78,351,001 WWOX
    esv2670748copy number variation204estd199human GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597 SCAPER
    esv2664803copy number variation436estd199human GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597 SCAPER
    esv2659318copy number variation40estd199human GRCh37 chr2: 66,185,965-66,197,059 , GRCh38.p12 chr2: 65,958,831-65,969,925 LINC02934
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