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 187

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904223copy number variation1nstd209human GRCh38 chr4: 70,293,358-70,421,488 , GRCh37.p13 chr4: 71,159,075-71,287,205 SMR3B, SMR3A, 2 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
    nsv5840099copy number variation2nstd209human GRCh38 chr4: 70,402,072-70,403,171 , GRCh37.p13 chr4: 71,267,789-71,268,888 OPRPN
    nsv5839475copy number variation1nstd209human GRCh38 chr4: 70,382,372-70,421,575 , GRCh37.p13 chr4: 71,248,089-71,287,292 SMR3B, OPRPN
    nsv5716250mobile element insertion1nstd211human GRCh38 chr4: 70,398,062-70,398,062 , GRCh37.p13 chr4: 71,263,779-71,263,779 OPRPN
    nsv5681490mobile element insertion2nstd211human GRCh38 chr4: 70,397,904-70,397,904 , GRCh37.p13 chr4: 71,263,621-71,263,621 OPRPN
    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
    nsv5605804insertion1nstd207human GRCh38 chr4: 70,397,890-70,397,890 , GRCh37.p13 chr4: 71,263,607-71,263,607 OPRPN
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5400929mobile element insertion1nstd206human GRCh38 chr4: 70,397,904-70,397,955 , GRCh37.p13 chr4: 71,263,621-71,263,672 OPRPN
    nsv5173033mobile element insertion1nstd203human GRCh38 chr4: 70,398,050-70,398,062 , GRCh37.p13 chr4: 71,263,767-71,263,779 OPRPN
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4922867copy number variation1nstd200human GRCh38 chr4: 70,401,427-70,401,496 , GRCh37.p13 chr4: 71,267,144-71,267,213 OPRPN
    nsv4922866copy number variation1nstd200human GRCh38 chr4: 70,398,741-70,400,166 , GRCh37.p13 chr4: 71,264,458-71,265,883 OPRPN
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4800135copy number variation1nstd200human GRCh37 chr4: 71,159,074-71,287,206 , GRCh38.p12 chr4: 70,293,357-70,421,489 CABS1, OPRPN, 2 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
    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