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Results: 1 to 20 of 46

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1067915complex1nstd51humanPathogenic GRCh38 (hg38) chr3: 50,302,170-50,302,206 , GRCh37 (hg19) chr3: 50,339,601-50,339,637 , GRCh37.p13 chr3|NW_003871059.1: 72,018-72,054 HYAL1
    nsv1014256copy number variation1nstd100human NCBI36 (hg18) chr3: 50,162,650-50,329,020 , GRCh37 (hg19) chr3: 50,187,646-50,354,016 , GRCh37.p13 chr3|NW_003871059.1: 1-86,433 , GRCh38 (hg38) chr3: 50,150,213-50,316,585 SEMA3F-AS1, SEMA3B-AS1, 13 more genes
    esv3512811copy number variation2estd59human NCBI36 (hg18) chr3: 50,317,052-50,324,000 , GRCh37.p13 chr3|NW_003871059.1: 74,465-81,413 , GRCh37 (hg19) chr3: 50,342,048-50,348,996 , GRCh38 (hg38) chr3: 50,304,617-50,311,565 HYAL1
    esv3512812copy number variation1estd59human NCBI36 (hg18) chr3: 50,317,052-50,324,000 , GRCh37.p13 chr3|NW_003871059.1: 74,465-81,413 , GRCh37 (hg19) chr3: 50,342,048-50,348,996 , GRCh38 (hg38) chr3: 50,304,617-50,311,565 HYAL1
    esv3421618copy number variation8estd59human NCBI36 (hg18) chr3: 50,271,577-50,274,125 , GRCh37.p13 chr3|NW_003871059.1: 28,989-31,537 , GRCh37 (hg19) chr3: 50,296,573-50,299,121 , GRCh38 (hg38) chr3: 50,259,141-50,261,689 GNAI2
    esv3404854copy number variation8estd59human NCBI36 (hg18) chr3: 50,280,377-50,282,925 , GRCh37 (hg19) chr3: 50,305,373-50,307,921 , GRCh37.p13 chr3|NW_003871059.1: 37,789-40,338 , GRCh38 (hg38) chr3: 50,267,941-50,270,490 SEMA3B
    esv3398486copy number variation8estd59human NCBI36 (hg18) chr3: 50,298,002-50,300,700 , GRCh37 (hg19) chr3: 50,322,998-50,325,696 , GRCh37.p13 chr3|NW_003871059.1: 55,415-58,113 , GRCh38 (hg38) chr3: 50,285,567-50,288,265 LSMEM2, IFRD2
    esv3365284copy number variation2estd59human NCBI36 (hg18) chr3: 50,316,702-50,324,100 , GRCh37.p13 chr3|NW_003871059.1: 74,115-81,513 , GRCh37 (hg19) chr3: 50,341,698-50,349,096 , GRCh38 (hg38) chr3: 50,304,267-50,311,665 HYAL1
    esv3341924copy number variation8estd59human NCBI36 (hg18) chr3: 50,331,502-50,334,300 , GRCh37 (hg19) chr3: 50,356,498-50,359,296 , GRCh37.p13 chr3|NW_003871059.1: 88,915-91,713 , GRCh38 (hg38) chr3: 50,319,067-50,321,865 HYAL2
    esv2759148copy number variation1estd1human NCBI35 (hg17) chr3: 50,173,482-50,346,381 , GRCh37.p13 chr3|NW_003871059.1: 1-100,694 , GRCh37 (hg19) chr3: 50,198,478-50,371,377 , GRCh38 (hg38) chr3: 50,161,045-50,333,946 SEMA3B-AS1, MIR5787, 15 more genes
    esv2757870copy number variation3estd1human NCBI35 (hg17) chr3: 50,173,482-50,346,381 , GRCh37.p13 chr3|NW_003871059.1: 1-100,694 , GRCh37 (hg19) chr3: 50,198,478-50,371,377 , GRCh38 (hg38) chr3: 50,161,045-50,333,946 SEMA3B-AS1, MIR5787, 15 more genes
    esv29569sequence alteration1estd20human NCBI36 (hg18) chr3: 50,318,470-50,324,352 , GRCh37 (hg19) chr3: 50,343,466-50,349,348 , GRCh37.p13 chr3|NW_003871059.1: 75,883-81,765 , GRCh38 (hg38) chr3: 50,306,035-50,311,917 HYAL1
    esv12015copy number variation1estd20human NCBI36 (hg18) chr3: 50,318,470-50,324,352 , GRCh37 (hg19) chr3: 50,343,466-50,349,348 , GRCh37.p13 chr3|NW_003871059.1: 75,883-81,765 , GRCh38 (hg38) chr3: 50,306,035-50,311,917 HYAL1
    nsv876777copy number variation1nstd71human NCBI36 (hg18) chr3: 50,316,330-50,343,095 , GRCh37.p13 chr3|NW_003871059.1: 73,743-100,508 , GRCh37 (hg19) chr3: 50,341,326-50,368,091 , GRCh38 (hg38) chr3: 50,303,895-50,330,660 RASSF1, TUSC2, 2 more genes
    nsv876776copy number variation1nstd71human NCBI36 (hg18) chr3: 50,316,330-50,337,375 , GRCh37 (hg19) chr3: 50,341,326-50,362,371 , GRCh37.p13 chr3|NW_003871059.1: 73,743-94,788 , GRCh38 (hg38) chr3: 50,303,895-50,324,940 TUSC2, HYAL1, 1 more genes
    nsv876774copy number variation1nstd71human NCBI36 (hg18) chr3: 50,267,197-50,411,831 , GRCh37.p13 chr3|NW_003871059.1: 24,609-100,694 , GRCh37 (hg19) chr3: 50,292,193-50,436,827 , GRCh38 (hg38) chr3: 50,254,761-50,399,396 SEMA3B-AS1, RASSF1-AS1, 16 more genes
    nsv876772copy number variation1nstd71human NCBI36 (hg18) chr3: 50,230,309-50,411,831 , GRCh37.p13 chr3|NW_003871059.1: 1-100,694 , GRCh37 (hg19) chr3: 50,255,305-50,436,827 , GRCh38 (hg38) chr3: 50,217,873-50,399,396 SEMA3B-AS1, RASSF1-AS1, 18 more genes
    esv1708957insertion1estd22human NCBI36 (hg18) chr3: 50,266,886-50,266,886 , GRCh37.p13 chr3|NW_003871059.1: 24,298-24,298 , GRCh37 (hg19) chr3: 50,291,882-50,291,882 , GRCh38 (hg38) chr3: 50,254,450-50,254,450 GNAI2
    esv1652979copy number variation1estd22human NCBI36 (hg18) chr3: 50,275,708-50,275,711 , GRCh37 (hg19) chr3: 50,300,704-50,300,707 , GRCh37.p13 chr3|NW_003871059.1: 33,120-33,123 , GRCh38 (hg38) chr3: 50,263,272-50,263,275 0
    esv1554945copy number variation1estd22human NCBI36 (hg18) chr3: 50,253,371-50,253,372 , GRCh37.p13 chr3|NW_003871059.1: 10,783-10,784 , GRCh37 (hg19) chr3: 50,278,367-50,278,368 , GRCh38 (hg38) chr3: 50,240,935-50,240,936 GNAI2

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