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 528

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114415mobile element insertion1nstd186human GRCh37 chr17: 53,116,104-53,116,155 , GRCh38.p12 chr17: 55,038,743-55,038,794 STXBP4
    nsv5978567insertion1nstd209human GRCh38 chr17: 55,038,729-55,038,729 , GRCh37.p13 chr17: 53,116,090-53,116,090 STXBP4
    nsv5971416insertion1nstd209human GRCh38 chr17: 55,011,508-55,011,508 , GRCh37.p13 chr17: 53,088,869-53,088,869 STXBP4
    nsv5941440copy number variation1nstd209human GRCh38 chr17: 55,106,396-55,106,489 , GRCh37.p13 chr17: 53,183,757-53,183,850 STXBP4
    nsv5941223copy number variation1nstd209human GRCh38 chr17: 55,049,207-55,054,867 , GRCh37.p13 chr17: 53,126,568-53,132,228 STXBP4
    nsv5936817copy number variation1nstd209human GRCh38 chr17: 55,166,591-55,177,025 , GRCh37.p13 chr17: 53,243,952-53,254,386 STXBP4
    nsv5881966copy number variation1nstd209human GRCh38 chr17: 55,049,179-55,054,297 , GRCh37.p13 chr17: 53,126,540-53,131,658 STXBP4
    nsv5880364copy number variation1nstd209human GRCh38 chr17: 55,166,859-55,175,224 , GRCh37.p13 chr17: 53,244,220-53,252,585 STXBP4
    nsv5724824mobile element insertion1nstd211human GRCh38 chr17: 55,096,682-55,096,682 , GRCh37.p13 chr17: 53,174,043-53,174,043 LOC107985002, STXBP4
    nsv5722348mobile element insertion2nstd211human GRCh38 chr17: 55,169,755-55,169,755 , GRCh37.p13 chr17: 53,247,116-53,247,116 STXBP4
    nsv5705846mobile element insertion1nstd211human GRCh38 chr17: 55,150,016-55,150,016 , GRCh37.p13 chr17: 53,227,377-53,227,377 STXBP4
    nsv5704274mobile element insertion1nstd211human GRCh38 chr17: 55,170,410-55,170,410 , GRCh37.p13 chr17: 53,247,771-53,247,771 STXBP4
    nsv5702172mobile element insertion1nstd211human GRCh38 chr17: 55,113,167-55,113,167 , GRCh37.p13 chr17: 53,190,528-53,190,528 STXBP4
    nsv5701219mobile element insertion2nstd211human GRCh38 chr17: 55,038,743-55,038,743 , GRCh37.p13 chr17: 53,116,104-53,116,104 STXBP4
    nsv5660396insertion1nstd207human GRCh38 chr17: 55,038,729-55,038,729 , GRCh37.p13 chr17: 53,116,090-53,116,090 STXBP4
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5544827insertion1nstd206human GRCh38 chr17: 55,150,016-55,150,051 , GRCh37.p13 chr17: 53,227,377-53,227,412 STXBP4
    nsv5533707copy number variation1nstd206human GRCh38 chr17: 55,044,780-55,044,851 , GRCh37.p13 chr17: 53,122,141-53,122,212 STXBP4
    nsv5529332copy number variation1nstd206human GRCh38 chr17: 54,631,610-54,997,284 , GRCh37.p13 chr17: 52,708,971-53,074,645 , COX11, 4 more genes
    nsv5519800copy number variation1nstd206human GRCh38 chr17: 55,166,591-55,177,029 , GRCh37.p13 chr17: 53,243,952-53,254,390 STXBP4
    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