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Items: 1 to 20 of 4281

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3829074copy number variation24estd219human GRCh37 chr3: 4,126,030-4,259,632 , GRCh38.p12 chr3: 4,084,346-4,217,948 SUMF1
    esv3830173copy number variation520estd219human GRCh37 chr3: 46,803,577-46,851,159 , GRCh38.p12 chr3: 46,762,087-46,809,669 PRSS44P
    esv3829072copy number variation17estd219human GRCh37 chr3: 4,115,225-4,163,698 , GRCh38.p12 chr3: 4,073,541-4,122,014 SUMF1
    esv3829075copy number variation20estd219human GRCh37 chr3: 4,132,878-4,173,500 , GRCh38.p12 chr3: 4,091,194-4,131,816 SUMF1
    esv3884482copy number variation2409estd219human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3870498copy number variation1037estd219human GRCh37 chr13: 57,752,516-57,781,577 , GRCh38.p12 chr13: 57,178,382-57,207,443 MTCO2P3
    esv3821789copy number variation1062estd219human GRCh37 chr1: 196,735,895-196,764,940 , GRCh38.p12 chr1: 196,766,765-196,795,810 CFHR3
    esv3821155copy number variation879estd219human GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586 NME7
    esv3883166copy number variation2estd219human GRCh37 chr19: 15,678,072-15,697,315 , GRCh38.p12 chr19: 15,567,261-15,586,504 CYP4F23P
    esv3849507copy number variation27estd219human GRCh37 chr7: 56,804,315-56,822,416 , GRCh38.p12 chr7: 56,736,622-56,754,723 LOC728416
    esv3862224copy number variation147estd219human GRCh37 chr10: 122,769,702-122,787,504 , GRCh38.p12 chr10: 121,010,189-121,027,991 LOC105378521
    esv3860443copy number variation1029estd219human GRCh37 chr10: 47,983,067-48,000,904 , GRCh38.p12 chr10: 50,168,602-50,186,441 ASAH2
    esv3827261copy number variation1244estd219human GRCh37 chr2: 180,064,283-180,083,019 , GRCh38.p12 chr2: 179,199,556-179,218,292 SESTD1
    esv3852311copy number variation601estd219human GRCh37 chr8: 2,250,517-2,266,603 , GRCh38.p12 chr8|NT_187576.1: 485,727-501,813 LOC105377783
    esv3850674copy number variation206estd219human GRCh37 chr7: 102,351,450-102,367,324 , GRCh38.p12 chr7: 102,711,003-102,726,877 RASA4DP
    esv3829073copy number variation13estd219human GRCh37 chr3: 4,116,837-4,131,808 , GRCh38.p12 chr3: 4,075,153-4,090,124 SUMF1
    esv3833727copy number variation624estd219human GRCh37 chr3: 195,456,936-195,471,412 , GRCh38.p12 chr3|NT_187688.1: 50,160-64,603 , GRCh38.p12 chr3|NT_187689.1: 100,562-115,038 , GRCh38.p12 chr3|NT_187690.1: 50,159-64,610 , GRCh38.p12 chr3|NT_187691.1: 50,266-64,780 , GRCh38.p12 chr3|NT_187532.1: 100,562-115,038 , GRCh38.p12 chr3: 195,730,065-195,744,541 , GRCh38.p12 chr3|NT_187678.1: 51,460-65,948 , GRCh38.p12 chr3|NT_187649.1: 50,164-64,603 MUC20
    esv3848710copy number variation14estd219human GRCh37 chr7: 24,300,411-24,314,236 , GRCh38.p12 chr7: 24,260,792-24,274,617 LOC107986777
    esv3851121copy number variation53estd219human GRCh37 chr7: 119,374,544-119,386,625 , GRCh38.p12 chr7: 119,734,490-119,746,571 LINC02476
    esv3836089copy number variation34estd219human GRCh37 chr4: 90,580,409-90,592,233 , GRCh38.p12 chr4: 89,659,258-89,671,082 LOC105377329
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