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 231

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975135inversion1nstd209human GRCh38 chr18: 10,627,041-12,196,370 , GRCh37.p13 chr18: 10,627,038-12,196,369 , GNAL, 28 more genes
    nsv5943609copy number variation1nstd209human GRCh38 chr18: 10,661,988-10,662,324 , GRCh37.p13 chr18: 10,661,985-10,662,321 LOC101927410
    nsv5672896copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,656,075-13,885,536 , GRCh38.p12 chr18: 2,656,076-13,885,537 RN7SL862P, LOC105371972, 181 more genes
    nsv5349867translocation1nstd200human GRCh38 chr18: 10,661,990-10,661,990 , GRCh38 chr18: 10,662,325-10,662,325 , GRCh37.p13 chr18: 10,661,987-10,661,987 , GRCh37.p13 chr18: 10,662,322-10,662,322 LOC101927410
    nsv5338528translocation1nstd200human GRCh37 chr18: 10,662,322-10,662,322 , GRCh37 chr18: 10,661,987-10,661,987 , GRCh38.p12 chr18: 10,661,990-10,661,990 , GRCh38.p12 chr18: 10,662,325-10,662,325 LOC101927410
    nsv4730028copy number variation1nstd102humanUncertain significance GRCh37 chr18: 10,025,171-11,295,845 , GRCh38.p12 chr18: 10,025,174-11,295,846 KIAA0895LP1, NAPG, 15 more genes
    nsv4729915copy number variation1nstd102humanPathogenic GRCh37 chr18: 7,598,173-15,422,644 , GRCh38.p12 chr18: 7,598,175-15,410,899 CEP192, RNU2-27P, 155 more genes
    nsv4684313copy number variation1nstd102humanUncertain significance GRCh37 chr18: 10,140,629-12,236,187 , GRCh38.p12 chr18: 10,140,632-12,236,188 PIEZO2, LOC105371986, 38 more genes
    nsv4679992copy number variation1nstd189human GRCh37.p13 chr18: 10,591,818-11,366,233 , GRCh38.p12 chr18: 10,591,821-11,366,234 , PIEZO2, 10 more genes
    nsv4679177copy number variation1nstd189human GRCh37.p13 chr18: 10,591,818-11,372,355 , GRCh38.p12 chr18: 10,591,821-11,372,356 , PIEZO2, 10 more genes
    nsv4676396copy number variation1nstd102humanPathogenic GRCh37 chr18: 971,295-11,250,447 , GRCh38.p12 chr18: 971,294-11,250,448 LOC100129774, LOC100419892, 146 more genes
    nsv4676393copy number variation1nstd102humanPathogenic GRCh37 chr18: 13,034-15,330,525 , GRCh38.p12 chr18: 13,034-15,330,526 PRELID3A, ANKRD30B, 275 more genes
    nsv4676314copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,304-15,143,714 , GRCh38.p12 chr18: 136,304-15,143,715 EIF4A2P1, PMM2P2, 263 more genes
    nsv4676159copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-13,894,429 , GRCh38.p12 chr18: 136,226-13,894,430 SLC25A51P2, BOLA2P1, 221 more genes
    nsv4676141copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-18,529,578 , GRCh38.p12 chr18: 136,226-20,949,617 ANKRD12, DLGAP1-AS1, 270 more genes
    nsv4626650copy number variation1nstd183human GRCh37 chr18: 10,593,600-11,923,379 , GRCh38.p12 chr18: 10,593,603-11,923,380 , MIX23P1, 22 more genes
    nsv4385858copy number variation1nstd173human GRCh37 chr18: 136,227-18,529,578 , GRCh38.p12 chr18: 136,227-20,949,617 , LOC105371995, 276 more genes
    nsv4348774copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-15,175,005 , GRCh38.p12 chr18: 136,226-15,175,006 ANKRD62, LOC100419892, 263 more genes
    nsv4264724copy number variation1nstd166human GRCh37.p13 chr18: 10,661,987-10,662,322 , GRCh38.p12 chr18: 10,661,990-10,662,325 LOC101927410
    nsv4257816copy number variation1nstd166human GRCh37.p13 chr18: 10,667,023-10,674,133 , GRCh38.p12 chr18: 10,667,026-10,674,136 LOC101927410, PIEZO2
    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