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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3133518copy number variation1nstd151human GRCh37 (hg19) chr3: 11,850,988-11,888,115 , GRCh38 (hg38) chr3: 11,809,514-11,846,641 , GRCh38.p2 chr3|NW_003871060.2: 141,778-173,151 TAMM41
    nsv3124838copy number variation1nstd151human GRCh37 (hg19) chr3: 11,871,185-11,888,115 , GRCh38 (hg38) chr3: 11,829,711-11,846,641 , GRCh38.p2 chr3|NW_003871060.2: 141,778-158,708 TAMM41
    nsv3120717copy number variation2nstd151human GRCh37 (hg19) chr3: 11,831,976-11,888,115 , GRCh38 (hg38) chr3: 11,790,502-11,846,641 , GRCh38.p2 chr3|NW_003871060.2: 141,778-173,151 TAMM41
    nsv3080652mobile element insertion1nstd144human GRCh37 (hg19) chr3: 11,876,693-11,876,693 , GRCh38.p2 chr3|NW_003871060.2: 153,200-153,200 , GRCh38 (hg38) chr3: 11,835,219-11,835,219 TAMM41
    esv3829319mobile element insertion63estd219human GRCh37 (hg19) chr3: 11,911,947-11,911,947 , GRCh38 (hg38) chr3: 11,870,473-11,870,473 , GRCh38.p2 chr3|NW_003871060.2: 115,986-115,986 FANCD2P2
    esv3829320copy number variation2estd219human GRCh37 (hg19) chr3: 11,919,452-11,923,242 , GRCh38 (hg38) chr3: 11,877,978-11,881,768 , GRCh38.p2 chr3|NW_003871060.2: 104,730-108,504 FANCD2P2
    esv3829322copy number variation18estd219human GRCh37 (hg19) chr3: 11,975,453-11,976,141 , GRCh38.p2 chr3|NW_003871060.2: 51,831-52,519 , GRCh38 (hg38) chr3: 11,933,979-11,934,667 0
    esv3829321copy number variation1estd219human GRCh37 (hg19) chr3: 11,956,494-11,958,096 , GRCh38 (hg38) chr3: 11,915,020-11,916,622 , GRCh38.p2 chr3|NW_003871060.2: 69,876-71,478 0
    esv3989674copy number variation1estd229human GRCh37 (hg19) chr3: 11,950,878-11,955,986 , GRCh38.p2 chr3|NW_003871060.2: 71,986-77,094 , GRCh38 (hg38) chr3: 11,909,404-11,914,512 0
    esv3989673copy number variation2estd229human GRCh37 (hg19) chr3: 11,950,878-11,955,986 , GRCh38 (hg38) chr3: 11,909,404-11,914,512 , GRCh38.p2 chr3|NW_003871060.2: 71,986-77,094 0
    esv3989677copy number variation1estd229human GRCh37 (hg19) chr3: 11,956,181-11,957,005 , GRCh38 (hg38) chr3: 11,914,707-11,915,531 , GRCh38.p2 chr3|NW_003871060.2: 70,967-71,791 0
    esv3989672copy number variation3estd229human GRCh37 (hg19) chr3: 11,950,840-11,955,948 , GRCh38 (hg38) chr3: 11,909,366-11,914,474 , GRCh38.p2 chr3|NW_003871060.2: 72,024-77,132 0
    esv3989676copy number variation2estd229human GRCh37 (hg19) chr3: 11,954,129-11,957,005 , GRCh38 (hg38) chr3: 11,912,655-11,915,531 , GRCh38.p2 chr3|NW_003871060.2: 70,967-73,843 0
    nsv2206566short tandem repeat2nstd128human GRCh37 (hg19) chr3: 12,025,147-12,025,163 , GRCh38 (hg38) chr3: 11,983,673-11,983,689 , GRCh38.p2 chr3|NW_003871060.2: 2,809-2,825 0
    nsv2206561short tandem repeat1nstd128human GRCh37 (hg19) chr3: 12,018,342-12,018,356 , GRCh38.p2 chr3|NW_003871060.2: 9,616-9,630 , GRCh38 (hg38) chr3: 11,976,868-11,976,882 0
    nsv2206557short tandem repeat2nstd128human GRCh37 (hg19) chr3: 12,011,048-12,011,073 , GRCh38 (hg38) chr3: 11,969,574-11,969,599 , GRCh38.p2 chr3|NW_003871060.2: 16,899-16,924 0
    nsv2206551short tandem repeat6nstd128human GRCh37 (hg19) chr3: 12,009,086-12,009,125 , GRCh38 (hg38) chr3: 11,967,612-11,967,651 , GRCh38.p2 chr3|NW_003871060.2: 18,847-18,886 0
    nsv2206522short tandem repeat3nstd128human GRCh37 (hg19) chr3: 11,991,897-11,991,919 , GRCh38.p2 chr3|NW_003871060.2: 36,053-36,075 , GRCh38 (hg38) chr3: 11,950,423-11,950,445 0
    nsv2206507short tandem repeat5nstd128human GRCh37 (hg19) chr3: 11,982,748-11,982,763 , GRCh38 (hg38) chr3: 11,941,274-11,941,289 , GRCh38.p2 chr3|NW_003871060.2: 45,209-45,224 0
    nsv2206473short tandem repeat2nstd128human GRCh37 (hg19) chr3: 11,948,176-11,948,188 , GRCh38 (hg38) chr3: 11,906,702-11,906,714 , GRCh38.p2 chr3|NW_003871060.2: 79,784-79,796 0
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