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 260

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5893450copy number variation1nstd209human GRCh38 chr5: 10,233,565-10,233,636 , GRCh37.p13 chr5: 10,233,677-10,233,748 ATPSCKMT
    nsv5889302copy number variation1nstd209human GRCh38 chr5: 10,246,265-10,247,914 , GRCh37.p13 chr5: 10,246,377-10,248,026 ATPSCKMT
    nsv5840841copy number variation1nstd209human GRCh38 chr5: 10,225,189-10,226,194 , GRCh37.p13 chr5: 10,225,301-10,226,306 ATPSCKMT
    nsv5840287copy number variation2nstd209human GRCh38 chr5: 10,246,259-10,247,958 , GRCh37.p13 chr5: 10,246,371-10,248,070 ATPSCKMT, CCT5
    nsv5840286copy number variation1nstd209human GRCh38 chr5: 10,238,453-10,239,652 , GRCh37.p13 chr5: 10,238,565-10,239,764 ATPSCKMT
    nsv5840265copy number variation1nstd209human GRCh38 chr5: 10,237,453-10,238,752 , GRCh37.p13 chr5: 10,237,565-10,238,864 ATPSCKMT
    nsv5570695copy number variation1nstd207human GRCh38 chr5: 10,233,565-10,233,636 , GRCh37.p13 chr5: 10,233,677-10,233,748 ATPSCKMT
    nsv5465626copy number variation1nstd206human GRCh38 chr5: 10,233,566-10,233,637 , GRCh37.p13 chr5: 10,233,678-10,233,749 ATPSCKMT
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv5232850copy number variation1nstd204human GRCh38.p13 chr5: 10,248,601-10,254,600 , GRCh37.p13 chr5: 10,248,713-10,254,712 ATPSCKMT, CCT5
    nsv4946464copy number variation1nstd200human GRCh38 chr5: 10,223,883-10,225,664 , GRCh37.p13 chr5: 10,223,995-10,225,776 ATPSCKMT
    nsv4728985copy number variation1nstd102humanUncertain significance GRCh37 chr5: 10,140,764-10,671,308 , GRCh38.p12 chr5: 10,140,652-10,671,196 MARCHF6, RPL30P7, 13 more genes
    nsv4685752copy number variation1nstd102humanPathogenic GRCh37 chr5: 71,904-22,078,969 , GRCh38.p12 chr5: 71,789-22,078,860 LINC01377, LOC100421308, 277 more genes
    nsv4674497copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-14,738,180 , GRCh38.p12 chr5: 113,461-14,738,071 LOC101929003, MTCYBP37, 192 more genes
    nsv4674444copy number variation1nstd102humanPathogenic GRCh37 chr5: 1,322,680-10,762,544 , GRCh38.p12 chr5: 1,322,565-10,762,432 LOC100132773, LINC01019, 125 more genes
    nsv4674161copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-23,364,376 , GRCh38.p12 chr5: 113,461-23,364,267 LOC102723561, LOC107986397, 287 more genes
    nsv4674130copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-11,767,720 , GRCh38.p12 chr5: 113,461-11,767,608 SLC9A3-AS1, LINC02114, 169 more genes
    nsv4522617copy number variation1nstd166human GRCh37.p13 chr5: 10,233,678-10,233,749 , GRCh38.p12 chr5: 10,233,566-10,233,637 ATPSCKMT
    nsv4477506mobile element insertion1nstd166human GRCh37.p13 chr5: 10,241,789-10,241,789 , GRCh38.p12 chr5: 10,241,677-10,241,677 ATPSCKMT
    nsv4457061copy number variation1nstd102humanUncertain significance GRCh37 chr5: 10,186,394-10,983,657 , GRCh38.p12 chr5: 10,186,282-10,983,545 ATPSCKMT, ROPN1L-AS1, 18 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