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 316

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148204copy number variation1nstd102humanPathogenic GRCh38 chr5: 9,999-14,320,000 , GRCh37.p13 chr5: 10,001-14,320,109 LOC105379638, LOC100420683, 185 more genes
    nsv7147885copy number variation1nstd232human GRCh37.p13 chr5: 10,258,415-10,258,496 , GRCh38.p12 chr5: 10,258,303-10,258,384 CCT5
    nsv7098841copy number variation1nstd102humanPathogenic GRCh37 chr5: 10,149,255-18,180,300 , GRCh38.p12 chr5: 10,149,143-18,180,191 RN7SKP133, TAF11L1, 102 more genes
    nsv7096744copy number variation1nstd102humanUncertain significance GRCh37 chr5: 10,250,453-10,264,895 , GRCh38.p12 chr5: 10,250,341-10,264,783 CCT5, ATPSCKMT
    nsv7056892inversion1nstd229human GRCh38 chr5: 10,258,111-10,261,558 , GRCh37.p13 chr5: 10,258,223-10,261,670 CCT5
    nsv7052860inversion1nstd229human GRCh38 chr5: 10,170,489-10,504,221 , GRCh37.p13 chr5: 10,170,601-10,504,333 CMBL, MIR10397, 11 more genes
    nsv7045933inversion1nstd229human GRCh38 chr5: 9,205,469-10,383,964 , GRCh37.p13 chr5: 9,205,581-10,384,076 SEMA5A-AS1, SNORD123, 15 more genes
    nsv6766002copy number variation1nstd229human GRCh38 chr5: 10,203,601-10,797,600 , GRCh37.p13 chr5: 10,203,713-10,797,712 LOC645763, DAP, 16 more genes
    nsv6765511copy number variation1nstd229human GRCh38 chr5: 10,137,393-10,304,241 , GRCh37.p13 chr5: 10,137,505-10,304,353 CMBL, ATPSCKMT, 1 more genes
    nsv6764486copy number variation1nstd229human GRCh38 chr5: 9,477,059-10,373,440 , GRCh37.p13 chr5: 9,477,171-10,373,552 LOC107986405, MARCHF6-DT, 15 more genes
    nsv6760731copy number variation1nstd229human GRCh38 chr5: 10,265,755-10,270,079 , GRCh37.p13 chr5: 10,265,867-10,270,191 CCT5
    nsv6760326copy number variation1nstd229human GRCh38 chr5: 10,260,500-10,265,871 , GRCh37.p13 chr5: 10,260,612-10,265,983 CCT5
    nsv6637149copy number variation1nstd102humanPathogenic GRCh37 chr5: 8,081,005-22,210,970 , GRCh38.p12 chr5: 8,080,892-22,210,861 LOC107986376, MARCHF11, 150 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 more genes
    nsv6636849copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-17,654,787 , GRCh38.p12 chr5: 113,462-17,654,678 ADCY2, HMGB3P3, 248 more genes
    nsv6636672copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-26,164,852 , GRCh38.p12 chr5: 113,462-26,164,743 LINC02123, LINC01020, 302 more genes
    nsv6636606copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420 BASP1, RNU1-76P, 338 more genes
    nsv6393580copy number variation1nstd223human GRCh38 chr5: 10,265,749-10,270,078 , GRCh37.p13 chr5: 10,265,861-10,270,190 CCT5
    nsv6315441copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-29,310,520 , GRCh38.p12 chr5: 113,461-29,310,413 FBXL7, LOC105374608, 319 more genes
    nsv6315416copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-30,712,376 , GRCh38.p12 chr5: 113,461-30,712,269 LOC105374649, LINC02196, 333 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