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Items: 1 to 20 of 61187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3775343copy number variation1estd192human GRCh37 chr5: 11,236,563-12,104,345 , GRCh38.p12 chr5: 11,236,451-12,104,233 CTNND2
    esv3803141copy number variation1estd192human GRCh37 chr4: 125,672,816-126,375,641 , GRCh38.p12 chr4: 124,751,661-125,454,486 FAT4
    esv3762702copy number variation1estd192human GRCh37 chr4: 33,100,161-33,717,194 , GRCh38.p12 chr4: 33,098,539-33,715,572 LOC105374391
    esv3811992copy number variation1estd192human GRCh37 chr13: 55,668,998-56,253,074 , GRCh38.p12 chr13: 55,094,863-55,678,940 MIR5007
    esv3781932copy number variation1estd192human GRCh37 chr13: 65,686,636-66,257,013 , GRCh38.p12 chr13: 65,112,504-65,682,881 STARP1
    esv3810884copy number variation1estd192human GRCh37 chr2: 117,834,729-118,401,491 , GRCh38.p12 chr2: 117,077,153-117,643,915 RNU7-190P
    esv3756127copy number variation1estd192human GRCh37 chr2: 205,809,792-206,359,903 , GRCh38.p12 chr2: 204,945,069-205,495,179 PARD3B
    esv3787342copy number variation1estd192human GRCh37 chr18: 25,540,575-26,047,179 , GRCh38.p12 chr18: 27,960,611-28,467,215 CDH2
    esv3801001copy number variation2estd192human GRCh37 chr11: 78,376,891-78,863,591 , GRCh38.p12 chr11: 78,665,846-79,152,546 TENM4
    esv3806786copy number variation1estd192human GRCh37 chr3: 84,226,973-84,704,722 , GRCh38.p12 chr3: 84,177,822-84,655,571 LINC00971
    esv3769730copy number variation1estd192human GRCh37 chr9: 10,065,611-10,542,891 , GRCh38.p12 chr9: 10,065,611-10,542,891 PTPRD
    esv3788188copy number variation1estd192human GRCh37 chr8: 85,078,662-85,544,499 , GRCh38.p12 chr8: 84,166,427-84,632,264 RALYL
    esv3783326copy number variation1estd192human GRCh37 chr8: 116,284,222-116,723,079 , GRCh38.p12 chr8: 115,271,993-115,710,852 TRPS1
    esv3788639copy number variation1estd192human GRCh37 chr4: 116,117,730-116,555,733 , GRCh38.p12 chr4: 115,196,574-115,634,577 RPF2P2
    esv3759763copy number variation1estd192human GRCh37 chr15: 54,895,946-55,327,611 , GRCh38.p12 chr15: 54,603,748-55,035,413 UNC13C
    esv3766700copy number variation1estd192human GRCh37 chr2: 50,379,340-50,787,199 , GRCh38.p12 chr2: 50,152,202-50,560,061 NRXN1
    esv3768428copy number variation2estd192human GRCh37 chr6: 124,477,413-124,876,467 , GRCh38.p12 chr6: 124,156,268-124,555,321 NKAIN2
    esv3814158copy number variation1estd192human GRCh37 chr4: 125,995,630-126,368,192 , GRCh38.p12 chr4: 125,074,475-125,447,037 FAT4
    esv3779073copy number variation1estd192human GRCh37 chr17: 69,235,538-69,607,917 , GRCh38.p12 chr17: 71,239,397-71,611,776 RNU7-155P
    esv3808154copy number variation4estd192human GRCh37 chr2: 205,505,327-205,876,998 , GRCh38.p12 chr2: 204,640,604-205,012,275 PARD3B
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