U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 3109

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5380701translocation1nstd200human GRCh38 chr2: 206,949,465-206,949,465 , GRCh38 chr3: 182,931,149-182,931,149 , GRCh37.p13 chr3: 182,648,937-182,648,937 , GRCh37.p13 chr2: 207,814,189-207,814,189 CPO
    nsv5380691translocation1nstd200human GRCh38 chr18: 21,936,902-21,936,902 , GRCh38 chr2: 143,253,676-143,253,676 , GRCh37.p13 chr2: 144,011,245-144,011,245 , GRCh37.p13 chr18: 19,516,863-19,516,863 ARHGAP15
    nsv5380668translocation1nstd200human GRCh38 chr20: 30,502,235-30,502,235 , GRCh38 chr2: 132,270,832-132,270,832 , GRCh37.p13 chr: NaN-NaN , GRCh37.p13 chr2: 133,028,405-133,028,405 LOC105373622
    nsv5380667translocation1nstd200human GRCh38 chr2: 132,243,527-132,243,527 , GRCh38 chr14: 18,223,596-18,223,596 , GRCh37.p13 chr14: 19,000,073-19,000,073 , GRCh37.p13 chr2: 133,001,100-133,001,100 ANKRD30BL
    nsv5380655translocation1nstd200human GRCh38 chr2: 128,728,715-128,728,715 , GRCh38 chr3: 129,847,305-129,847,305 , GRCh37.p13 chr3: 129,566,148-129,566,148 , GRCh37.p13 chr2: 129,486,289-129,486,289 TMCC1
    nsv5380635translocation1nstd200human GRCh38 chr2: 124,557,827-124,557,827 , GRCh38 chrX: 73,412,452-73,412,452 , GRCh37.p13 chrX: 72,632,288-72,632,288 , GRCh37.p13 chr2: 125,315,404-125,315,404 CNTNAP5
    nsv5380634translocation1nstd200human GRCh38 chr2: 124,557,826-124,557,826 , GRCh38 chrX: 73,413,214-73,413,214 , GRCh37.p13 chr2: 125,315,403-125,315,403 , GRCh37.p13 chrX: 72,633,050-72,633,050 CNTNAP5
    nsv5380631translocation1nstd200human GRCh38 chr2: 124,267,819-124,267,819 , GRCh38 chr4: 136,292,704-136,292,704 , GRCh37.p13 chr2: 125,025,396-125,025,396 , GRCh37.p13 chr4: 137,213,859-137,213,859 CNTNAP5
    nsv5380606translocation1nstd200human GRCh38 chr2: 119,536,509-119,536,509 , GRCh38 chr3: 54,849,050-54,849,050 , GRCh37.p13 chr2: 120,294,085-120,294,085 , GRCh37.p13 chr3: 54,883,077-54,883,077 CACNA2D3
    nsv5380602translocation1nstd200human GRCh38 chr6: 56,892,986-56,892,986 , GRCh38 chr2: 118,892,936-118,892,936 , GRCh37.p13 chr6: 56,757,784-56,757,784 , GRCh37.p13 chr2: 119,650,512-119,650,512 DST
    nsv5380590translocation1nstd200human GRCh38 chrX: 33,761,262-33,761,262 , GRCh38 chr2: 116,127,363-116,127,363 , GRCh37.p13 chrX: 33,779,379-33,779,379 , GRCh37.p13 chr2: 116,884,939-116,884,939 LOC105373153
    nsv5380544translocation1nstd200human GRCh38 chr2: 98,047,743-98,047,743 , GRCh38 chr4: 74,413,719-74,413,719 , GRCh37.p13 chr4: 75,279,436-75,279,436 , GRCh37.p13 chr2: 98,664,206-98,664,206 LOC105373501
    nsv5380518translocation1nstd200human GRCh38 chr2: 91,996,405-91,996,405 , GRCh38 chr9: 5,231,296-5,231,296 , GRCh37.p13 chr2: 92,184,431-92,184,431 , GRCh37.p13 chr9: 5,231,296-5,231,296 INSL4
    nsv5380498translocation1nstd200human GRCh38 chr9: 69,616,532-69,616,532 , GRCh38 chr2: 88,271,625-88,271,625 , GRCh37.p13 chr2: 88,571,144-88,571,144 , GRCh37.p13 chr9: 72,231,448-72,231,448 APBA1
    nsv5380476translocation1nstd200human GRCh38 chr1: 28,189,162-28,189,162 , GRCh38 chr19: 23,845,132-23,845,132 , GRCh37.p13 chr19: 24,027,934-24,027,934 , GRCh37.p13 chr1: 28,515,673-28,515,673 PTAFR
    nsv5380475translocation1nstd200human GRCh38 chr2: 83,622,922-83,622,922 , GRCh38 chr8: 72,881,772-72,881,772 , GRCh37.p13 chr8: 73,794,007-73,794,007 , GRCh37.p13 chr2: 83,850,046-83,850,046 KCNB2
    nsv5380327translocation1nstd200human GRCh38 chrX: 117,497,478-117,497,478 , GRCh38 chr19: 57,600,536-57,600,536 , GRCh37.p13 chrX: 116,631,441-116,631,441 , GRCh37.p13 chr19: 58,111,904-58,111,904 ZNF530
    nsv5380303translocation1nstd200human GRCh38 chrX: 11,713,871-11,713,871 , GRCh38 chr19: 52,556,951-52,556,951 , GRCh37.p13 chr19: 53,060,204-53,060,204 , GRCh37.p13 chrX: 11,731,991-11,731,991 ZNF808
    nsv5380285translocation1nstd200human GRCh38 chr20: 38,378,085-38,378,085 , GRCh38 chr19: 47,758,862-47,758,862 , GRCh37.p13 chr20: 37,006,727-37,006,727 , GRCh37.p13 chr19: 48,262,119-48,262,119 NOP53-AS1
    nsv5380231translocation1nstd200human GRCh38 chr2: 39,572,265-39,572,265 , GRCh38 chr7: 121,417,993-121,417,993 , GRCh37.p13 chr2: 39,799,405-39,799,405 , GRCh37.p13 chr7: 121,058,047-121,058,047 MAP4K3-DT
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center