U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 435

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096765copy number variation1nstd102humanUncertain significance GRCh37 chr5: 171,765,373-172,939,426 , GRCh38.p12 chr5: 172,338,369-173,512,423 MIR5003, LOC285591, 31 more genes
    nsv7057944inversion1nstd229human GRCh38 chr5: 172,134,356-176,589,266 , GRCh37.p13 chr5: 171,561,360-176,016,267 MIR10523, NIFKP2, 92 more genes
    nsv7049449inversion1nstd229human GRCh38 chr5: 172,453,794-172,456,998 , GRCh37.p13 chr5: 171,880,798-171,884,002 SH3PXD2B
    nsv7047615inversion1nstd229human GRCh38 chr5: 172,361,077-172,361,091 , GRCh37.p13 chr5: 171,788,081-171,788,095 SH3PXD2B
    nsv7045921inversion1nstd229human GRCh38 chr5: 172,324,995-172,325,980 , GRCh37.p13 chr5: 171,751,999-171,752,984 SH3PXD2B
    nsv7042814inversion1nstd229human GRCh38 chr5: 172,449,497-172,454,146 , GRCh37.p13 chr5: 171,876,501-171,881,150 SH3PXD2B
    nsv7041481inversion1nstd229human GRCh38 chr5: 172,382,193-172,382,928 , GRCh37.p13 chr5: 171,809,197-171,809,932 SH3PXD2B
    nsv7038947inversion1nstd229human GRCh38 chr5: 172,419,311-172,420,826 , GRCh37.p13 chr5: 171,846,315-171,847,830 SH3PXD2B
    nsv6794614copy number variation1nstd229human GRCh38 chr5: 172,345,126-172,345,184 , GRCh37.p13 chr5: 171,772,130-171,772,188 SH3PXD2B
    nsv6793196copy number variation1nstd229human GRCh38 chr5: 172,345,038-172,345,122 , GRCh37.p13 chr5: 171,772,042-171,772,126 SH3PXD2B
    nsv6791689copy number variation1nstd229human GRCh38 chr5: 172,378,505-172,384,174 , GRCh37.p13 chr5: 171,805,509-171,811,178 SH3PXD2B
    nsv6785893copy number variation1nstd229human GRCh38 chr5: 172,370,526-172,443,430 , GRCh37.p13 chr5: 171,797,530-171,870,434 SH3PXD2B
    nsv6784105copy number variation1nstd229human GRCh38 chr5: 172,397,301-172,399,400 , GRCh37.p13 chr5: 171,824,305-171,826,404 SH3PXD2B
    nsv6782955copy number variation1nstd229human GRCh38 chr5: 172,218,701-173,333,400 , GRCh37.p13 chr5: 171,645,705-172,760,403 ATP6V0E1, MIR10523, 31 more genes
    nsv6781923copy number variation1nstd229human GRCh38 chr5: 172,429,079-172,456,257 , GRCh37.p13 chr5: 171,856,083-171,883,261 SH3PXD2B
    nsv6781917copy number variation1nstd229human GRCh38 chr5: 172,401,340-172,404,515 , GRCh37.p13 chr5: 171,828,344-171,831,519 SH3PXD2B
    nsv6781511copy number variation1nstd229human GRCh38 chr5: 170,662,244-174,111,903 , GRCh37.p13 chr5: 170,089,248-173,538,906 LOC101928093, LOC107986482, 79 more genes
    nsv6780483copy number variation1nstd229human GRCh38 chr5: 172,373,837-172,386,374 , GRCh37.p13 chr5: 171,800,841-171,813,378 SH3PXD2B
    nsv6779758copy number variation1nstd229human GRCh38 chr5: 172,365,958-172,372,158 , GRCh37.p13 chr5: 171,792,962-171,799,162 SH3PXD2B
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    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