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 165

    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
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7098818copy number variation1nstd102humanPathogenic GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956 LOC105374542, PPARGC1A, 232 more genes
    nsv7096981copy number variation1nstd102humanUncertain significance GRCh37 chr4: 13,371,500-13,546,038 , GRCh38.p12 chr4: 13,369,876-13,544,414 LINC01097, LINC01096, 3 more genes
    nsv6735664copy number variation1nstd229human GRCh38 chr4: 13,486,278-13,567,746 , GRCh37.p13 chr4: 13,487,902-13,569,370 LINC01097, NKX3-2, 3 more genes
    nsv6733000copy number variation1nstd229human GRCh38 chr4: 13,466,501-13,637,500 , GRCh37.p13 chr4: 13,468,125-13,639,124 LINC01097, MIR5091, 6 more genes
    nsv6732009copy number variation1nstd229human GRCh38 chr4: 13,174,270-14,155,070 , GRCh37.p13 chr4: 13,175,894-14,156,694 LOC101929048, HSP90AB2P, 14 more genes
    nsv6731857copy number variation1nstd229human GRCh38 chr4: 13,341,201-13,599,300 , GRCh37.p13 chr4: 13,342,825-13,600,924 NKX3-2, LINC01097, 4 more genes
    nsv6730266copy number variation1nstd229human GRCh38 chr4: 11,584,151-13,998,677 , GRCh37.p13 chr4: 11,585,775-14,000,301 LINC02270, LINC02360, 24 more genes
    nsv6729388copy number variation1nstd229human GRCh38 chr4: 13,534,950-13,542,104 , GRCh37.p13 chr4: 13,536,574-13,543,728 NKX3-2
    nsv6723385copy number variation1nstd229human GRCh38 chr4: 13,544,917-13,544,945 , GRCh37.p13 chr4: 13,546,541-13,546,569 LINC01096, NKX3-2
    nsv6723208copy number variation1nstd229human GRCh38 chr4: 5,355,032-14,502,279 , GRCh37.p13 chr4: 5,356,759-14,503,903 OR7E86P, LINC02447, 164 more genes
    nsv6719304copy number variation1nstd229human GRCh38 chr4: 13,205,984-13,626,731 , GRCh37.p13 chr4: 13,207,608-13,628,355 LINC01097, LINC01096, 6 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
    nsv6368324copy number variation1nstd223human GRCh38 chr4: 11,584,151-13,998,677 , GRCh37.p13 chr4: 11,585,775-14,000,301 LOC105374495, LOC107986182, 24 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
    nsv6315347copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,964,575 , GRCh38.p12 chr4: 68,453-20,962,952 LOC100421802, ADRA2C, 375 more genes
    nsv6291097copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,587,167 , GRCh38.p12 chr4: 68,453-20,585,544 LOC105374479, LOC105374502, 372 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