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 174

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5890071copy number variation1nstd209human GRCh38 chr4: 17,613,295-17,613,637 , GRCh37.p13 chr4: 17,614,918-17,615,260 MED28
    nsv5716094mobile element insertion1nstd211human GRCh38 chr4: 17,623,436-17,623,436 , GRCh37.p13 chr4: 17,625,059-17,625,059 MED28
    nsv5682405mobile element insertion1nstd211human GRCh38 chr4: 17,620,168-17,620,168 , GRCh37.p13 chr4: 17,621,791-17,621,791 MED28
    nsv5408759mobile element insertion1nstd206human GRCh38 chr4: 17,620,168-17,620,219 , GRCh37.p13 chr4: 17,621,791-17,621,842 MED28
    nsv5176242mobile element insertion1nstd203human GRCh38 chr4: 17,623,398-17,623,436 , GRCh37.p13 chr4: 17,625,021-17,625,059 MED28
    nsv5099634mobile element insertion1nstd203human GRCh38 chr4: 17,632,058-17,632,058 , GRCh37.p13 chr4: 17,633,681-17,633,681 FAM184B, MED28
    nsv5083619mobile element insertion1nstd203human GRCh38 chr4: 17,632,043-17,632,058 , GRCh37.p13 chr4: 17,633,666-17,633,681 FAM184B, MED28
    nsv5081772mobile element insertion1nstd203human GRCh38 chr4: 17,620,154-17,620,168 , GRCh37.p13 chr4: 17,621,777-17,621,791 MED28
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4925339copy number variation1nstd200human GRCh38 chr4: 17,613,731-17,614,028 , GRCh37.p13 chr4: 17,615,354-17,615,651 MED28
    nsv4925333copy number variation1nstd200human GRCh38 chr4: 16,822,715-17,819,702 , GRCh37.p13 chr4: 16,824,338-17,821,325 LDB2, LINC02493, 14 more genes
    nsv4921738copy number variation1nstd200human GRCh38 chr4: 17,613,193-17,623,128 , GRCh37.p13 chr4: 17,614,816-17,624,751 MED28
    nsv4809066copy number variation1nstd200human GRCh37 chr4: 16,824,339-17,821,325 , GRCh38.p12 chr4: 16,822,716-17,819,702 LOC105374507, CLRN2, 14 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