Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 159

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3156047copy number variation1nstd151human GRCh37 (hg19) chr13: 76,432,054-76,445,065 , GRCh38 (hg38) chr13: 75,857,918-75,870,929 LMO7DN, LMO7
    nsv3146401copy number variation1nstd151human GRCh37 (hg19) chr13: 76,381,614-76,445,065 , GRCh38 (hg38) chr13: 75,807,478-75,870,929 LMO7DN, LMO7
    nsv3143375copy number variation1nstd151human GRCh37 (hg19) chr13: 70,370,867-76,445,065 , GRCh38 (hg38) chr13: 69,796,735-75,870,929 LMO7DN, KLF12, 58 more genes
    nsv3109785copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr13: 67,522,431-114,110,750 , GRCh37 (hg19) chr13: 68,624,430-115,085,141 , GRCh38 (hg38) chr13: 68,050,298-114,327,173 LMO7DN, NALCN, 567 more genes
    nsv2779196copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr13: 53,932,358-96,586,363 , GRCh38 (hg38) chr13: 53,358,223-95,934,109 , NCBI36 (hg18) chr13: 52,830,359-95,384,364 LMO7DN, LINC00557, 407 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 LMO7DN, PARP1P1, 1325 more genes
    nsv2778080copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr13: 53,551,300-109,850,651 , GRCh38 (hg38) chr13: 52,977,165-109,198,303 , NCBI36 (hg18) chr13: 52,449,301-108,648,652 LMO7DN, KLF5, 580 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 LMO7DN, KLF5, 585 more genes
    nsv2776490copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr13: 61,686,543-83,302,092 , GRCh38 (hg38) chr13: 61,112,409-82,727,957 , NCBI36 (hg18) chr13: 60,584,544-82,200,093 LMO7DN, KLF5, 218 more genes
    nsv2775465copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr13: 61,424,168-115,107,733 , GRCh38 (hg38) chr13: 60,850,034-114,342,258 , NCBI36 (hg18) chr13: 60,322,169-114,125,835 LMO7DN, KLF5, 635 more genes
    nsv2775178copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr13: 56,431,743-115,107,733 , GRCh38 (hg38) chr13: 55,857,609-114,342,258 , NCBI36 (hg18) chr13: 55,329,744-114,125,835 LMO7DN, LOC105370300, 686 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 LMO7DN, ATP4B, 1349 more genes
    nsv2771753copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr13: 72,174,742-82,221,361 , GRCh38 (hg38) chr13: 71,600,610-81,647,226 , NCBI36 (hg18) chr13: 71,072,743-81,119,362 LMO7DN, CLN5, 126 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 LMO7DN, LOC105370361, 1357 more genes
    nsv2769036copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr13: 71,871,468-115,107,733 , GRCh38 (hg38) chr13: 71,297,336-114,342,258 , NCBI36 (hg18) chr13: 70,769,469-114,125,835 LMO7DN, MIR17HG, 546 more genes
    nsv2768216copy-neutral loss of heterozygosity1nstd125human GRCh38 (hg38) chr13: 73,851,090-79,043,551 , GRCh37 (hg19) chr13: 74,425,227-79,617,686 LMO7DN, BTF3P11, 71 more genes
    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 LMO7DN, PARP1P1, 1121 more genes
    nsv1713265short tandem repeat5nstd128human GRCh37 (hg19) chr13: 76,445,383-76,445,431 , GRCh38 (hg38) chr13: 75,871,247-75,871,295 LMO7DN
    nsv1712258short tandem repeat1nstd128human GRCh37 (hg19) chr13: 76,445,441-76,445,464 , GRCh38 (hg38) chr13: 75,871,305-75,871,328 LMO7DN
    nsv1712013short tandem repeat13nstd128human GRCh37 (hg19) chr13: 76,453,475-76,453,516 , GRCh38 (hg38) chr13: 75,879,339-75,879,380 LMO7DN, LMO7DN-IT1
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Search details

    See more...

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center