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 120

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5942783copy number variation1nstd209human GRCh38 chr17: 28,594,998-28,595,485 , GRCh37.p13 chr17: 26,922,016-26,922,503 SPAG5
    nsv5696677mobile element insertion1nstd211human GRCh38 chr17: 28,581,463-28,581,463 , GRCh37.p13 chr17: 26,908,481-26,908,481 SPAG5
    nsv5418740mobile element insertion1nstd206human GRCh38 chr17: 28,581,463-28,581,514 , GRCh37.p13 chr17: 26,908,481-26,908,532 SPAG5
    nsv5023902copy number variation1nstd200human GRCh38 chr17: 28,371,101-28,759,758 , GRCh37.p13 chr17: 26,840,020-27,086,776 RSKR, TRAF4, 26 more genes
    nsv5010256copy number variation1nstd200human GRCh38 chr17: 28,599,271-28,601,021 , GRCh37.p13 chr17: 26,926,289-26,928,039 SPAG5, SPAG5-AS1
    nsv5010255copy number variation1nstd200human GRCh38 chr17: 28,594,950-28,597,607 , GRCh37.p13 chr17: 26,921,968-26,924,625 SPAG5, SPAG5-AS1
    nsv4858464copy number variation1nstd200human GRCh37 chr17: 26,922,230-26,924,330 , GRCh38.p12 chr17: 28,595,212-28,597,312 SPAG5-AS1, SPAG5
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675321copy number variation1nstd102humanPathogenic GRCh37 chr17: 25,274,363-28,450,707 , GRCh38.p12 chr17: 26,947,337-30,123,689 ABHD15, LOC100420408, 112 more genes
    nsv4673397copy number variation1nstd186human GRCh37 chr17: 26,915,773-26,916,428 , GRCh38.p12 chr17: 28,588,755-28,589,410 SPAG5
    nsv4668549copy number variation1nstd186human GRCh37 chr17: 26,922,422-26,923,109 , GRCh38.p12 chr17: 28,595,404-28,596,091 SPAG5
    nsv4630643copy number variation2nstd183human GRCh37 chr17: 26,922,422-26,923,109 , GRCh38.p12 chr17: 28,595,404-28,596,091 SPAG5
    nsv4629934copy number variation1nstd183human GRCh37 chr17: 26,915,773-26,916,428 , GRCh38.p12 chr17: 28,588,755-28,589,410 SPAG5
    nsv4573528mobile element insertion1nstd166human GRCh37.p13 chr17: 26,919,782-26,919,782 , GRCh38.p12 chr17: 28,592,764-28,592,764 SPAG5
    nsv4532694copy number variation1nstd166human GRCh37.p13 chr17: 26,743,508-26,954,563 , GRCh38.p12 chr17: 28,416,490-28,627,545 SLC13A2, LOC101060112, 10 more genes
    nsv4514475mobile element insertion1nstd166human GRCh37.p13 chr17: 26,921,033-26,921,033 , GRCh38.p12 chr17: 28,594,015-28,594,015 SPAG5
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4379025copy number variation1nstd173human GRCh37 chr17: 25,307,567-27,710,963 , GRCh38.p12 chr17: 26,980,541-29,383,945 , MIR451A, 91 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4249957copy number variation1nstd166human GRCh37.p13 chr17: 26,921,962-26,924,630 , GRCh38.p12 chr17: 28,594,944-28,597,612 SPAG5, SPAG5-AS1
    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