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 284

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974139inversion1nstd209human GRCh38 chr10: 50,135,648-50,227,658 , GRCh37.p13 chr10: 51,895,408-51,987,418 SLC9A3P1, ASAH2
    nsv5864121copy number variation1nstd209human GRCh38 chr10: 50,194,325-50,197,949 , GRCh37.p13 chr10: 51,954,085-51,957,709 ASAH2
    nsv5718850mobile element insertion1nstd211human GRCh38 chr10: 50,226,386-50,226,386 , GRCh37.p13 chr10: 51,986,146-51,986,146 ASAH2
    nsv5714135mobile element insertion1nstd211human GRCh38 chr10: 50,199,278-50,199,278 , GRCh37.p13 chr10: 51,959,038-51,959,038 ASAH2
    nsv5712238mobile element insertion1nstd211human GRCh38 chr10: 50,194,419-50,194,419 , GRCh37.p13 chr10: 51,954,179-51,954,179 ASAH2
    nsv5701008mobile element insertion1nstd211human GRCh38 chr10: 50,238,192-50,238,192 , GRCh37.p13 chr10: 51,997,952-51,997,952 ASAH2
    nsv5556403mobile element insertion1nstd206human GRCh38 chr10: 50,226,386-50,226,437 , GRCh37.p13 chr10: 51,986,146-51,986,197 ASAH2
    nsv5488937copy number variation1nstd206human GRCh38 chr10: 50,238,112-50,238,197 , GRCh37.p13 chr10: 51,997,872-51,997,957 ASAH2
    nsv5487892copy number variation1nstd206human GRCh38 chr10: 50,194,517-50,194,586 , GRCh37.p13 chr10: 51,954,277-51,954,346 ASAH2
    nsv5483515copy number variation1nstd206human GRCh38 chr10: 47,586,000-50,754,368 , GRCh37.p13 chr10: 46,591,857-52,514,128 HMGB1P50, PARG, 65 more genes
    nsv5413878mobile element insertion1nstd206human GRCh38 chr10: 50,238,192-50,238,243 , GRCh37.p13 chr10: 51,997,952-51,998,003 ASAH2
    nsv5412402mobile element insertion1nstd206human GRCh38 chr10: 50,194,419-50,194,470 , GRCh37.p13 chr10: 51,954,179-51,954,230 ASAH2
    nsv5410185mobile element insertion1nstd206human GRCh38 chr10: 50,199,278-50,199,329 , GRCh37.p13 chr10: 51,959,038-51,959,089 ASAH2
    nsv5260096copy number variation1nstd204human GRCh38.p13 chr10: 50,181,197-50,183,219 , GRCh37.p13 chr10: 51,940,957-51,942,979 ASAH2
    nsv5259903copy number variation1nstd204human GRCh38.p13 chr10: 50,192,312-50,244,054 , GRCh37.p13 chr10: 51,952,072-52,003,814 ASAH2
    nsv5259698copy number variation1nstd204human GRCh38.p13 chr10: 50,182,864-50,186,179 , GRCh37.p13 chr10: 51,942,624-51,945,939 ASAH2
    nsv5259648copy number variation1nstd204human GRCh38.p13 chr10: 50,210,425-50,244,654 , GRCh37.p13 chr10: 51,970,185-52,004,414 ASAH2
    nsv5258641copy number variation1nstd204human GRCh38.p13 chr10: 50,206,901-50,209,200 , GRCh37.p13 chr10: 51,966,661-51,968,960 ASAH2
    nsv5257192copy number variation1nstd204human GRCh38.p13 chr10: 50,196,260-50,199,236 , GRCh37.p13 chr10: 51,956,020-51,958,996 ASAH2
    nsv5256886copy number variation1nstd204human GRCh38.p13 chr10: 50,179,734-50,185,598 , GRCh37.p13 chr10: 51,939,494-51,945,358 ASAH2
    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