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 227

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973931inversion1nstd209human GRCh38 chr4: 68,852,162-69,022,295 , GRCh37.p13 chr4: 69,717,880-69,888,013 UGT2B27P, UGT2A3, 6 more genes
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 147 more genes
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5560956sequence alteration1nstd206human GRCh38 chr4: 68,883,815-69,126,528 , GRCh37.p13 chr4: 69,749,533-69,992,246 UGT2B27P, SPOPLP1, 10 more genes
    nsv5554461sequence alteration1nstd206human GRCh38 chr4: 68,827,323-69,009,082 , GRCh37.p13 chr4: 69,693,041-69,874,800 UGT2B10, UGT2A3, 5 more genes
    nsv5458546copy number variation1nstd206human GRCh38 chr4: 68,940,430-68,946,845 , GRCh37.p13 chr4: 69,806,148-69,812,563 UGT2A3
    nsv5455438copy number variation1nstd206human GRCh38 chr4: 68,936,749-68,942,322 , GRCh37.p13 chr4: 69,802,467-69,808,040 UGT2A3
    nsv5315999copy number variation1nstd204human GRCh38.p13 chr4: 68,945,472-68,952,178 , GRCh37.p13 chr4: 69,811,190-69,817,896 UGT2A3
    nsv5229416copy number variation1nstd204human GRCh38.p13 chr4: 68,946,195-68,953,499 , GRCh37.p13 chr4: 69,811,913-69,819,217 UGT2A3
    nsv5229379copy number variation1nstd204human GRCh38.p13 chr4: 68,950,450-68,951,949 , GRCh37.p13 chr4: 69,816,168-69,817,667 UGT2A3
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4925757copy number variation1nstd200human GRCh38 chr4: 68,951,880-69,072,001 , GRCh37.p13 chr4: 69,817,598-69,937,719 UGT2B27P, UGT2A3, 6 more genes
    nsv4925756copy number variation1nstd200human GRCh38 chr4: 68,950,044-69,844,903 , GRCh37.p13 chr4: 69,815,762-70,710,621 LOC100422022, UGT2A2, 28 more genes
    nsv4925754copy number variation1nstd200human GRCh38 chr4: 68,795,160-69,345,433 , GRCh37.p13 chr4: 69,660,878-70,211,151 UGT2B28, SPOPLP3, 21 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 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