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 127

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7049186inversion1nstd229human GRCh38 chr4: 38,135,041-40,245,309 , GRCh37.p13 chr4: 38,136,662-40,246,929 SMIM14, RNU6-887P, 42 more genes
    nsv7040614inversion1nstd229human GRCh38 chr4: 39,608,359-40,081,859 , GRCh37.p13 chr4: 39,609,979-40,083,479 RN7SL558P, N4BP2, 11 more genes
    nsv7038584inversion1nstd229human GRCh38 chr4: 38,474,718-40,416,508 , GRCh37.p13 chr4: 38,476,339-40,418,525 RPL9, UBE2K, 41 more genes
    nsv6737060copy number variation1nstd229human GRCh38 chr4: 39,729,240-39,903,379 , GRCh37.p13 chr4: 39,730,860-39,904,999 PDS5A, ZBTB12BP, 2 more genes
    nsv6733200copy number variation1nstd229human GRCh38 chr4: 39,752,895-39,988,399 , GRCh37.p13 chr4: 39,754,515-39,990,019 PDS5A, ZBTB12BP, 4 more genes
    nsv6732166copy number variation1nstd229human GRCh38 chr4: 39,770,741-39,770,790 , GRCh37.p13 chr4: 39,772,361-39,772,410 ZBTB12BP, UBE2K
    nsv6726155copy number variation1nstd229human GRCh38 chr4: 39,630,360-40,250,301 , GRCh37.p13 chr4: 39,631,980-40,251,921 N4BP2, RNU6-1112P, 11 more genes
    nsv6719673copy number variation1nstd229human GRCh38 chr4: 39,701,678-40,111,180 , GRCh37.p13 chr4: 39,703,298-40,112,800 PABPC1P1, LOC344967, 8 more genes
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6629865copy number variation1nstd224human GRCh37 chr4: 39,748,523-39,835,826 , GRCh38.p12 chr4: 39,746,903-39,834,206 UBE2K, RN7SL558P, 2 more genes
    nsv6629443copy number variation1nstd224human GRCh37 chr4: 39,605,669-39,894,988 , GRCh38.p12 chr4: 39,604,049-39,893,368 UBE2K, PDS5A, 5 more genes
    nsv6393578copy number variation1nstd223human GRCh38 chr4: 39,729,240-39,903,379 , GRCh37.p13 chr4: 39,730,860-39,904,999 UBE2K, RN7SL558P, 2 more genes
    nsv6381801copy number variation1nstd223human GRCh38 chr4: 39,751,312-39,814,980 , GRCh37.p13 chr4: 39,752,932-39,816,600 ZBTB12BP, UBE2K, 1 more genes
    nsv6315440copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552 FAM86KP, ENPP7P11, 631 more genes
    nsv6312251copy number variation1nstd102humanUncertain significance GRCh37 chr4: 38,765,721-41,750,627 , GRCh38.p12 chr4: 38,764,100-41,748,610 RNU6-32P, SMIM14-DT, 52 more genes
    nsv6299237copy number variation1nstd186human GRCh37 chr4: 39,762,343-39,775,361 , GRCh38.p12 chr4: 39,760,723-39,773,741 UBE2K, ZBTB12BP, 1 more genes
    nsv6135081copy number variation1nstd213human GRCh37 chr4: 39,770,000-41,280,001 , GRCh38.p12 chr4: 39,768,380-41,277,984 APBB2, RHOH, 22 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