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 179

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946247copy number variation1nstd209human GRCh38 chr17: 43,008,147-43,008,641 , GRCh37.p13 chr17: 41,160,164-41,160,658 IFI35
    nsv5932664copy number variation1nstd209human GRCh38 chr17: 43,011,303-43,012,388 , GRCh37.p13 chr17: 41,163,320-41,164,405 IFI35
    nsv5869021copy number variation1nstd209human GRCh38 chr17: 43,011,228-43,012,327 , GRCh37.p13 chr17: 41,163,245-41,164,344 IFI35
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5530983copy number variation1nstd206human GRCh38 chr17: 43,005,793-43,006,152 , GRCh37.p13 chr17: 41,157,810-41,158,169 IFI35
    nsv5526931copy number variation1nstd206human GRCh38 chr17: 43,011,335-43,012,389 , GRCh37.p13 chr17: 41,163,352-41,164,406 IFI35
    nsv5374931translocation1nstd200human GRCh38 chr17: 43,011,372-43,011,372 , GRCh38 chr17: 43,012,389-43,012,389 , GRCh37.p13 chr17: 41,164,406-41,164,406 , GRCh37.p13 chr17: 41,163,389-41,163,389 IFI35
    nsv5323583copy number variation1nstd204human GRCh38.p13 chr17: 43,008,099-43,008,618 , GRCh37.p13 chr17: 41,160,116-41,160,635 IFI35
    nsv5287669copy number variation1nstd204human GRCh38.p13 chr17: 42,963,201-43,231,700 , GRCh37.p13 chr17: 41,115,218-41,383,489 PTGES3L, CCDC200, 15 more genes
    nsv5196998mobile element insertion1nstd203human GRCh38 chr17: 43,009,160-43,009,170 , GRCh37.p13 chr17: 41,161,177-41,161,187 IFI35
    nsv4867047copy number variation1nstd200human GRCh37 chr17: 41,163,363-41,164,415 , GRCh38.p12 chr17: 43,011,346-43,012,398 IFI35
    nsv4867046copy number variation1nstd200human GRCh37 chr17: 41,157,742-41,158,175 , GRCh38.p12 chr17: 43,005,725-43,006,158 IFI35
    nsv4745729copy number variation1nstd199human GRCh37 chr17: 41,163,339-41,164,426 , GRCh38.p12 chr17: 43,011,322-43,012,409 IFI35
    nsv4666775copy number variation1nstd186human GRCh37 chr17: 41,163,352-41,164,584 , GRCh38.p12 chr17: 43,011,335-43,012,567 IFI35
    nsv4630870copy number variation1nstd183human GRCh37 chr17: 41,163,352-41,164,584 , GRCh38.p12 chr17: 43,011,335-43,012,567 IFI35
    nsv4531597copy number variation1nstd166human GRCh37.p13 chr17: 41,163,352-41,164,406 , GRCh38.p12 chr17: 43,011,335-43,012,389 IFI35
    nsv4432525copy number variation1nstd172human GRCh37.p13 chr17: 41,163,353-41,164,406 , GRCh38.p12 chr17: 43,011,336-43,012,389 IFI35
    nsv4428119copy number variation1nstd174human GRCh37 chr17: 41,163,347-41,164,584 , GRCh38.p12 chr17: 43,011,330-43,012,567 IFI35
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4271726copy number variation1nstd166human GRCh37.p13 chr17: 41,157,604-41,167,801 , GRCh38.p12 chr17: 43,005,587-43,015,784 IFI35, VAT1
    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