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 311

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147273copy number variation1nstd232human GRCh37.p13 chr17: 80,016,128-80,016,213 , GRCh38.p12 chr17: 82,058,252-82,058,337 GPS1, DUS1L
    nsv7145484copy number variation1nstd232human GRCh37.p13 chr17: 80,014,848-80,014,925 , GRCh38.p12 chr17: 82,056,972-82,057,049 GPS1, DUS1L
    nsv7144253copy number variation1nstd232human GRCh37.p13 chr17: 80,014,265-80,014,342 , GRCh38.p12 chr17: 82,056,389-82,056,466 GPS1, DUS1L
    nsv7141312copy number variation1nstd232human GRCh37.p13 chr17: 80,014,423-80,014,500 , GRCh38.p12 chr17: 82,056,547-82,056,624 GPS1, DUS1L
    nsv7138387copy number variation1nstd232human GRCh37.p13 chr17: 80,014,640-80,014,712 , GRCh38.p12 chr17: 82,056,764-82,056,836 GPS1, DUS1L
    nsv7137846copy number variation1nstd232human GRCh37.p13 chr17: 80,012,684-80,012,770 , GRCh38.p12 chr17: 82,054,808-82,054,894 GPS1
    nsv7098933copy number variation1nstd102humanUncertain significance GRCh38 chr17: 82,004,063-83,087,346 , GRCh37.p13 chr17: 79,961,939-81,045,222 ZNF750, LINC01970, 37 more genes
    nsv7098715copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,539,041-81,052,322 , GRCh38.p12 chr17: 81,572,015-83,094,577 LOC105371939, LINC01970, 65 more genes
    nsv7095370copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,477,716-80,900,339 , GRCh38.p12 chr17: 81,510,690-82,942,463 MIR6787, TBCD, 67 more genes
    nsv7094997copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,891,090-80,333,370 , GRCh38.p12 chr17: 81,933,214-82,375,494 LOC105371939, LINC01970, 22 more genes
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv7064374inversion1nstd229human GRCh38 chr17: 82,046,151-82,149,895 , GRCh37.p13 chr17: 80,004,027-80,107,771 GPS1, CCDC57, 4 more genes
    nsv7061699inversion1nstd229human GRCh38 chr17: 81,983,159-82,059,180 , GRCh37.p13 chr17: 79,941,035-80,017,056 RAC3, CENPX, 7 more genes
    nsv6997997copy number variation1nstd229human GRCh38 chr17: 81,965,405-82,127,093 , GRCh37.p13 chr17: 79,923,281-80,084,969 ASPSCR1, CCDC57, 11 more genes
    nsv6989489copy number variation1nstd229human GRCh38 chr17: 81,929,777-82,073,240 , GRCh37.p13 chr17: 79,887,653-80,031,116 PYCR1, ASPSCR1, 12 more genes
    nsv6984488copy number variation1nstd229human GRCh38 chr17: 82,036,901-82,098,400 , GRCh37.p13 chr17: 79,994,777-80,056,276 SNORD134, GPS1, 5 more genes
    nsv6979040copy number variation1nstd229human GRCh38 chr17: 82,057,725-82,059,924 , GRCh37.p13 chr17: 80,015,601-80,017,800 DUS1L, GPS1
    nsv6533522copy number variation1nstd223human GRCh38 chr17: 82,052,201-82,542,400 , GRCh37.p13 chr17: 80,010,077-80,500,276 MIR6787, CD7, 19 more genes
    nsv6530652copy number variation1nstd223human GRCh38 chr17: 81,965,405-82,127,093 , GRCh37.p13 chr17: 79,923,281-80,084,969 RAC3, FASN, 11 more genes
    nsv6525507copy number variation1nstd223human GRCh38 chr17: 81,799,201-82,693,800 , GRCh37.p13 chr17: 79,759,050-80,651,676 CENPX, RFNG, 47 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