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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3156547copy number variation1nstd151human GRCh37 (hg19) chr13: 47,243,162-47,470,046 , GRCh38 (hg38) chr13: 46,669,027-46,895,911 ESD, HTR2A, 3 more genes
    nsv3152948copy number variation1nstd151human GRCh37 (hg19) chr13: 47,354,067-47,358,490 , GRCh38 (hg38) chr13: 46,779,932-46,784,355 ESD
    nsv3152318copy number variation1nstd151human GRCh37 (hg19) chr13: 46,937,248-51,519,673 , GRCh38 (hg38) chr13: 46,363,113-50,945,537 ESD, RCBTB2, 85 more genes
    nsv3151434copy number variation1nstd151human GRCh37 (hg19) chr13: 46,276,523-51,523,646 , GRCh38 (hg38) chr13: 45,702,388-50,949,510 ESD, FKBP1AP3, 100 more genes
    nsv3150690copy number variation1nstd151human GRCh37 (hg19) chr13: 47,224,333-47,365,553 , GRCh38 (hg38) chr13: 46,650,198-46,791,418 ESD, LOC107984563, 1 more genes
    nsv3150627copy number variation1nstd151human GRCh37 (hg19) chr13: 47,345,548-47,365,553 , GRCh38 (hg38) chr13: 46,771,413-46,791,418 ESD
    nsv3150391copy number variation1nstd151human GRCh37 (hg19) chr13: 47,243,162-47,365,553 , GRCh38 (hg38) chr13: 46,669,027-46,791,418 ESD, LRCH1, 1 more genes
    nsv3150302copy number variation1nstd151human GRCh37 (hg19) chr13: 47,243,162-47,466,730 , GRCh38 (hg38) chr13: 46,669,027-46,892,595 ESD, HTR2A, 3 more genes
    nsv3144827copy number variation1nstd151human GRCh37 (hg19) chr13: 47,345,548-47,351,763 , GRCh38 (hg38) chr13: 46,771,413-46,777,628 ESD
    nsv3141851copy number variation1nstd151human GRCh37 (hg19) chr13: 46,937,248-50,623,200 , GRCh38 (hg38) chr13: 46,363,113-50,049,064 ESD, RCBTB2, 73 more genes
    nsv3138727copy number variation1nstd151human GRCh37 (hg19) chr13: 47,297,353-47,466,730 , GRCh38 (hg38) chr13: 46,723,218-46,892,595 ESD, LRCH1, 3 more genes
    esv4010165copy number variation1estd233human GRCh37 (hg19) chr13: 45,296,000-48,497,000 , GRCh38 (hg38) chr13: 44,721,864-47,922,865 ESD, CPB2, 67 more genes
    nsv2787183copy number variation1nstd132human NCBI36 (hg18) chr13: 46,244,294-46,265,511 , GRCh37 (hg19) chr13: 47,346,293-47,367,510 , GRCh38 (hg38) chr13: 46,772,158-46,793,375 ESD
    nsv2783298copy number variation1nstd132human NCBI36 (hg18) chr13: 46,244,294-46,279,431 , GRCh37 (hg19) chr13: 47,346,293-47,381,430 , GRCh38 (hg38) chr13: 46,772,158-46,807,295 ESD
    nsv2782755copy number variation1nstd132human NCBI36 (hg18) chr13: 46,260,385-46,264,034 , GRCh37 (hg19) chr13: 47,362,384-47,366,033 , GRCh38 (hg38) chr13: 46,788,249-46,791,898 ESD
    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 ESD, PARP1P1, 1325 more genes
    nsv2778501copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr13: 47,312,129-51,342,279 , GRCh38 (hg38) chr13: 46,737,994-50,768,143 , NCBI36 (hg18) chr13: 46,210,130-50,240,280 ESD, SNRPGP14, 72 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 ESD, KLF5, 585 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 ESD, CPB2, 444 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 ESD, ATP4B, 1349 more genes
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