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 289

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5840288copy number variation1nstd209human GRCh38 chr5: 10,262,087-10,266,077 , GRCh37.p13 chr5: 10,262,199-10,266,189 CCT5
    nsv5840287copy number variation2nstd209human GRCh38 chr5: 10,246,259-10,247,958 , GRCh37.p13 chr5: 10,246,371-10,248,070 ATPSCKMT, CCT5
    nsv5726448mobile element insertion1nstd211human GRCh38 chr5: 10,252,885-10,252,885 , GRCh37.p13 chr5: 10,252,997-10,252,997 CCT5
    nsv5557811mobile element insertion1nstd206human GRCh38 chr5: 10,252,889-10,252,936 , GRCh37.p13 chr5: 10,253,001-10,253,048 CCT5
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv5304810copy number variation1nstd204human GRCh38.p13 chr5: 10,256,614-10,256,750 , GRCh37.p13 chr5: 10,256,726-10,256,862 CCT5
    nsv5232850copy number variation1nstd204human GRCh38.p13 chr5: 10,248,601-10,254,600 , GRCh37.p13 chr5: 10,248,713-10,254,712 ATPSCKMT, CCT5
    nsv4946465copy number variation1nstd200human GRCh38 chr5: 10,265,754-10,270,078 , GRCh37.p13 chr5: 10,265,866-10,270,190 CCT5
    nsv4792684copy number variation1nstd200human GRCh37 chr5: 10,265,866-10,270,190 , GRCh38.p12 chr5: 10,265,754-10,270,078 CCT5
    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
    nsv4523624copy number variation1nstd166human GRCh37.p13 chr5: 10,261,023-10,261,669 , GRCh38.p12 chr5: 10,260,911-10,261,557 CCT5
    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
    nsv4369315copy number variation1nstd173human GRCh37 chr5: 113,577-10,304,966 , GRCh38.p12 chr5: 113,462-10,304,854 , LOC105374625, 158 more genes
    nsv4349271copy number variation1nstd102humanPathogenic GRCh37 chr5: 140,474-26,906,925 , GRCh38.p12 chr5: 140,359-26,906,816 MIR4636, LRRC14B, 304 more genes
    nsv4125445copy number variation1nstd166human GRCh37.p13 chr5: 10,262,730-10,263,243 , GRCh38.p12 chr5: 10,262,618-10,263,131 CCT5
    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