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 138

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098766copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,806,534-56,540,597 , GRCh38.p12 chr17: 57,729,173-58,463,236 SRSF1, LOC105371840, 24 more genes
    nsv7068165inversion1nstd229human GRCh38 chr17: 58,272,314-58,274,976 , GRCh37.p13 chr17: 56,349,675-56,352,337 MPO
    nsv6996810copy number variation1nstd229human GRCh38 chr17: 58,280,395-58,289,392 , GRCh37.p13 chr17: 56,357,756-56,366,753 MPO
    nsv6992386copy number variation1nstd229human GRCh38 chr17: 58,271,109-58,271,147 , GRCh37.p13 chr17: 56,348,470-56,348,508 MPO
    nsv6988034copy number variation1nstd229human GRCh38 chr17: 57,983,239-58,340,473 , GRCh37.p13 chr17: 56,060,600-56,417,834 MIR4736, LOC105371841, 16 more genes
    nsv6634423copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,043,662-56,728,123 , GRCh38.p12 chr17: 56,966,301-58,650,762 RNU7-134P, DYNLL2-DT, 42 more genes
    nsv6594549inversion1nstd223human GRCh38 chr17: 58,274,643-58,275,014 , GRCh37.p13 chr17: 56,352,004-56,352,375 MPO
    nsv6580985inversion1nstd223human GRCh38 chr17: 58,274,641-58,275,030 , GRCh37.p13 chr17: 56,352,002-56,352,391 MPO
    nsv6310393copy number variation1nstd102humanUncertain significance GRCh37 chr17: 54,671,585-59,938,900 , GRCh38.p12 chr17: 56,594,224-61,861,539 RNF43, LOC107985048, 132 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5374969translocation1nstd200human GRCh38 chr17: 58,274,643-58,274,643 , GRCh38 chr17: 58,275,014-58,275,014 , GRCh37.p13 chr17: 56,352,004-56,352,004 , GRCh37.p13 chr17: 56,352,375-56,352,375 MPO
    nsv5374968translocation1nstd200human GRCh38 chr17: 58,274,980-58,274,980 , GRCh38 chr17: 58,272,314-58,272,314 , GRCh37.p13 chr17: 56,349,675-56,349,675 , GRCh37.p13 chr17: 56,352,341-56,352,341 MPO
    nsv5344864translocation1nstd200human GRCh37 chr17: 56,352,341-56,352,341 , GRCh37 chr17: 56,349,675-56,349,675 , GRCh38.p12 chr17: 58,272,314-58,272,314 , GRCh38.p12 chr17: 58,274,980-58,274,980 MPO
    nsv5342606translocation1nstd200human GRCh37 chr17: 56,352,004-56,352,004 , GRCh37 chr17: 56,352,375-56,352,375 , GRCh38.p12 chr17: 58,275,014-58,275,014 , GRCh38.p12 chr17: 58,274,643-58,274,643 MPO
    nsv4531949copy number variation1nstd166human GRCh37.p13 chr17: 56,348,110-56,348,185 , GRCh38.p12 chr17: 58,270,749-58,270,824 MPO
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv3914957copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,496,167-57,812,825 , GRCh38 chr17: 57,418,806-59,735,464 , NCBI36 chr17: 52,851,166-55,167,607 CLTC, LOC101927557, 67 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 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