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Items: 1 to 20 of 972

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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
    esv2676068copy number variation152estd199human GRCh37 chr6: 32,454,245-32,511,792 , GRCh38.p12 chr6: 32,486,468-32,544,015 HLA-DRB5
    esv2666277copy number variation79estd199human GRCh37 chr7: 141,765,351-141,794,383 , GRCh38.p12 chr7: 142,065,551-142,094,583 , GRCh38.p12 chr7|NT_187562.1: 27,431-56,463 MGAM
    esv2657599copy number variation40estd199human GRCh37 chr9: 44,742,045-44,764,392 , GRCh38.p12 chr9: 61,534,207-61,556,554 LOC105379437
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    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
    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
    esv2664165copy number variation220estd199human GRCh37 chr7: 100,327,572-100,340,716 , GRCh38.p12 chr7: 100,729,949-100,743,093 ZAN
    esv2659146copy number variation109estd199human GRCh37 chrX: 154,790,189-154,803,312 , GRCh38.p12 chrX: 155,560,528-155,573,651 TMLHE
    esv2664803copy number variation436estd199human GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597 SCAPER
    esv2673899copy number variation5estd199human GRCh37 chr1: 111,376,881-111,388,874 , GRCh38.p12 chr1: 110,834,259-110,846,252 NRBF2P3
    esv2663832copy number variation109estd199human GRCh37 chr4: 118,579,966-118,591,119 , GRCh38.p12 chr4: 117,658,811-117,669,964 LINC01378
    esv2674298copy number variation219estd199human GRCh37 chr1: 35,101,421-35,111,976 , GRCh38.p12 chr1: 34,635,820-34,646,375 LOC105378641
    esv2660604copy number variation109estd199human GRCh37 chr1: 35,101,421-35,111,976 , GRCh38.p12 chr1: 34,635,820-34,646,375 LOC105378641
    esv2673551copy number variation872estd199human GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616 VEZF1P1
    esv2675979copy number variation520estd199human GRCh37 chr6: 53,924,803-53,934,828 , GRCh38.p12 chr6: 54,060,005-54,070,030 MLIP
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