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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3154130copy number variation1nstd151human GRCh37 (hg19) chr13: 50,495,593-51,528,126 , GRCh38 (hg38) chr13: 49,921,457-50,953,990 DLEU2, MIR16-1, 17 more genes
    nsv3152318copy number variation1nstd151human GRCh37 (hg19) chr13: 46,937,248-51,519,673 , GRCh38 (hg38) chr13: 46,363,113-50,945,537 HTR2A, DLEU2, 85 more genes
    nsv3151434copy number variation1nstd151human GRCh37 (hg19) chr13: 46,276,523-51,523,646 , GRCh38 (hg38) chr13: 45,702,388-50,949,510 DLEU2, LPAR6, 100 more genes
    nsv3151167copy number variation3nstd151human GRCh37 (hg19) chr13: 50,586,068-51,523,646 , GRCh38 (hg38) chr13: 50,011,932-50,949,510 DLEU2, TRIM13, 15 more genes
    nsv3146667copy number variation1nstd151human GRCh37 (hg19) chr13: 51,501,540-51,509,140 , GRCh38 (hg38) chr13: 50,927,404-50,935,004 RNASEH2B
    nsv3146208copy number variation1nstd151human GRCh37 (hg19) chr13: 50,746,224-51,528,126 , GRCh38 (hg38) chr13: 50,172,088-50,953,990 DLEU1, RNASEH2B, 9 more genes
    nsv3141605copy number variation1nstd151human GRCh37 (hg19) chr13: 48,827,941-51,528,126 , GRCh38 (hg38) chr13: 48,253,805-50,953,990 RCBTB2, KPNA3, 55 more genes
    nsv3141007copy number variation1nstd151human GRCh37 (hg19) chr13: 51,287,351-51,603,792 , GRCh38 (hg38) chr13: 50,713,215-51,029,656 GUCY1B2, LOC107984567, 6 more genes
    nsv3139612copy number variation1nstd151human GRCh37 (hg19) chr13: 50,594,347-51,544,103 , GRCh38 (hg38) chr13: 50,020,211-50,969,967 RNASEH2B, ST13P4, 14 more genes
    nsv3139351copy number variation1nstd151human GRCh37 (hg19) chr13: 49,854,642-51,528,126 , GRCh38 (hg38) chr13: 49,280,506-50,953,990 KPNA3, DLEU1, 32 more genes
    nsv3139045copy number variation2nstd151human GRCh37 (hg19) chr13: 51,504,816-51,523,646 , GRCh38 (hg38) chr13: 50,930,680-50,949,510 RNASEH2B
    esv4010167copy number variation1estd233human GRCh37 (hg19) chr13: 48,520,000-55,877,000 , GRCh38 (hg38) chr13: 47,945,865-55,302,865 ST13P4, EBPL, 125 more genes
    nsv2778836copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr13: 19,231,330-114,127,980 , GRCh37 (hg19) chr13: 20,333,330-115,085,141 , GRCh38 (hg38) chr13: 19,759,190-114,344,403 MIR759, PLA2G12AP2, 1329 more genes
    nsv2777083copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr13: 42,457,841-91,796,698 , GRCh38 (hg38) chr13: 41,883,705-91,144,444 , NCBI36 (hg18) chr13: 41,355,841-90,594,699 NDFIP2-AS1, LOC105370210, 587 more genes
    nsv2772752copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr13: 32,946,120-62,698,217 , GRCh38 (hg38) chr13: 32,371,983-62,124,084 , NCBI36 (hg18) chr13: 31,844,120-61,596,218 RPS12P24, NDE1P2, 445 more genes
    nsv2772645copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr13: 48,906,943-52,778,614 , GRCh38 (hg38) chr13: 48,332,807-52,204,479 , NCBI36 (hg18) chr13: 47,804,944-51,676,615 FABP5P2, CDADC1, 86 more genes
    nsv2772506copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr13: 19,571,503-115,092,510 , GRCh38 (hg38) chr13: 18,997,363-114,327,035 , NCBI36 (hg18) chr13: 18,469,503-114,110,612 RN7SL60P, FGF14, 1353 more genes
    nsv2769532copy number variation5nstd37humanPathogenic GRCh37 (hg19) chr13: 19,436,287-115,107,733 , GRCh38 (hg38) chr13: 18,862,147-114,342,258 , NCBI36 (hg18) chr13: 18,334,287-114,125,835 HIST1H2APS6, LOC107984597, 1361 more genes
    esv3870338copy number variation2estd219human GRCh37 (hg19) chr13: 51,512,933-51,515,919 , GRCh38 (hg38) chr13: 50,938,797-50,941,783 RNASEH2B
    nsv2733538copy number variation1nstd130human NCBI36 (hg18) chr13: 28,932,813-114,121,252 , GRCh37 (hg19) chr13: 30,034,813-115,085,141 , GRCh38 (hg38) chr13: 29,460,676-114,337,675 PARP1P1, BTF3P11, 1124 more genes
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