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 156

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5894861copy number variation1nstd209human GRCh38 chr4: 55,350,125-55,350,259 , GRCh37.p13 chr4: 56,216,292-56,216,426 SRD5A3, FCF1P8
    nsv5690341mobile element insertion2nstd211human GRCh38 chr4: 55,344,598-55,344,598 , GRCh37.p13 chr4: 56,210,765-56,210,765 SRD5A3
    nsv5684246mobile element insertion1nstd211human GRCh38 chr4: 55,356,026-55,356,026 , GRCh37.p13 chr4: 56,222,193-56,222,193 SRD5A3
    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
    nsv5352801translocation1nstd200human GRCh38 chr4: 37,582,597-37,582,597 , GRCh38 chr4: 55,372,822-55,372,822 , GRCh37.p13 chr4: 37,584,219-37,584,219 , GRCh37.p13 chr4: 56,238,989-56,238,989 C4orf19, SRD5A3, 1 more genes
    nsv5333444translocation1nstd200human GRCh37 chr4: 56,238,989-56,238,989 , GRCh37 chr4: 37,584,219-37,584,219 , GRCh38.p12 chr4: 55,372,822-55,372,822 , GRCh38.p12 chr4: 37,582,597-37,582,597 C4orf19, SRD5A3, 1 more genes
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4913373copy number variation1nstd200human GRCh38 chr4: 55,345,052-55,351,255 , GRCh37.p13 chr4: 56,211,219-56,217,422 SRD5A3, FCF1P8
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4791871copy number variation1nstd200human GRCh37 chr4: 56,211,219-56,217,422 , GRCh38.p12 chr4: 55,345,052-55,351,255 FCF1P8, SRD5A3
    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
    nsv4558659mobile element insertion1nstd166human GRCh37.p13 chr4: 56,228,551-56,228,551 , GRCh38.p12 chr4: 55,362,384-55,362,384 SRD5A3
    nsv4103648copy number variation1nstd166human GRCh37.p13 chr4: 56,234,907-56,237,637 , GRCh38.p12 chr4: 55,368,740-55,371,470 SRD5A3, SRD5A3-AS1
    nsv4101795copy number variation1nstd166human GRCh37.p13 chr4: 56,222,160-56,228,337 , GRCh38.p12 chr4: 55,355,993-55,362,170 SRD5A3
    nsv4095621copy number variation1nstd166human GRCh37.p13 chr4: 56,226,118-56,226,455 , GRCh38.p12 chr4: 55,359,951-55,360,288 SRD5A3
    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