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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3972047copy number variation1nstd102humanUncertain significance GRCh38 (hg38) chr4: 1,002,780-1,002,806 , GRCh37.p13 chr4: 996,568-996,594 , NCBI36 (hg18) chr4: 986,568-986,594 IDUA
    nsv3972046copy number variation1nstd102humanLikely pathogenic GRCh38 (hg38) chr4: 1,000,886-1,000,886 , GRCh37.p13 chr4: 994,674-994,674 , NCBI36 (hg18) chr4: 984,674-984,674 IDUA
    nsv3929953copy number variation1nstd167human GRCh37 (hg19) chr4: 993,630-993,803 , GRCh38.p12 chr4: 999,842-1,000,015 IDUA
    nsv3924868copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr4: 36,424-1,956,092 , GRCh37.p13 chr4: 507,005-1,957,819 , NCBI36 (hg18) chr4: 26,424-1,927,617 IDUA, LETM1, 65 more genes
    nsv3924303copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr4: 72,555-4,888,108 , GRCh37.p13 chr4: 507,005-4,889,835 , NCBI36 (hg18) chr4: 62,447-4,940,736 IDUA, ADRA2C, 145 more genes
    nsv3924209copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr4: 72,555-10,250,666 , GRCh37.p13 chr4: 507,005-10,252,290 , NCBI36 (hg18) chr4: 62,447-9,861,388 IDUA, CTBP1, 278 more genes
    nsv3924013copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr4: 72,555-12,898,612 , GRCh37.p13 chr4: 507,005-12,900,236 , NCBI36 (hg18) chr4: 62,447-12,509,334 IDUA, ADD1, 310 more genes
    nsv3923597copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr4: 23,574-4,585,682 , GRCh37.p13 chr4: 33,574-4,534,781 , GRCh38.p12 chr4: 33,574-4,533,054 IDUA, GRK4, 141 more genes
    nsv3923472copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr4: 72,555-3,785,385 , GRCh37.p13 chr4: 507,005-3,787,112 , NCBI36 (hg18) chr4: 62,447-3,756,910 IDUA, GAK, 112 more genes
    nsv3923296copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr4: 72,555-28,066,309 , GRCh37.p13 chr4: 507,005-28,067,931 , NCBI36 (hg18) chr4: 62,447-27,677,029 IDUA, BST1, 470 more genes
    nsv3923243copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr4: 51,519-3,775,116 , GRCh37.p13 chr4: 507,005-3,776,843 , NCBI36 (hg18) chr4: 41,413-3,746,641 IDUA, ADD1, 113 more genes
    nsv3922676copy number variation1nstd102humanBenign/Likely benign GRCh38 (hg38) chr4: 958,618-1,026,629 , GRCh37.p13 chr4: 952,406-1,020,417 , NCBI36 (hg18) chr4: 942,406-1,010,417 IDUA, DGKQ, 3 more genes
    nsv3922123copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr4: 72,555-2,689,579 , GRCh37.p13 chr4: 507,005-2,691,306 , NCBI36 (hg18) chr4: 62,447-2,661,104 IDUA, GAK, 85 more genes
    nsv3922056copy number variation1nstd102humanUncertain significance GRCh38 (hg38) chr4: 72,555-1,581,567 , GRCh37.p13 chr4: 507,005-1,583,294 , NCBI36 (hg18) chr4: 62,447-1,553,260 IDUA, ZNF141, 55 more genes
    nsv3921949copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr4: 36,424-3,974,044 , GRCh37.p13 chr4: 507,005-3,975,771 , NCBI36 (hg18) chr4: 26,424-4,026,672 IDUA, ADRA2C, 120 more genes
    nsv3921088copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr4: 85,149-4,596,207 , GRCh37.p13 chr4: 507,005-4,597,934 , NCBI36 (hg18) chr4: 75,040-4,648,835 IDUA, ADRA2C, 141 more genes
    nsv3920869copy number variation1nstd102humanUncertain significance GRCh38 (hg38) chr4: 36,424-1,562,150 , GRCh37.p13 chr4: 507,005-1,563,877 , NCBI36 (hg18) chr4: 26,424-1,533,937 IDUA, GAK, 55 more genes
    nsv3920636copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr4: 51,519-8,222,798 , GRCh37.p13 chr4: 507,005-8,224,525 , NCBI36 (hg18) chr4: 41,413-8,275,425 IDUA, HGFAC, 204 more genes
    nsv3920609copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr4: 72,555-3,206,313 , GRCh37.p13 chr4: 507,005-3,208,040 , NCBI36 (hg18) chr4: 62,447-3,177,838 IDUA, FGFR3, 97 more genes
    nsv3920438copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr4: 78,578-3,363,219 , GRCh37.p13 chr4: 507,005-3,364,946 , NCBI36 (hg18) chr4: 68,470-3,334,744 IDUA, PDE6B, 101 more genes
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