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 396

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952572insertion1nstd209human GRCh38 chr7: 23,743,123-23,743,123 , GRCh37.p13 chr7: 23,782,742-23,782,742 STK31
    nsv5920694copy number variation1nstd209human GRCh38 chr7: 23,810,422-23,810,502 , GRCh37.p13 chr7: 23,850,041-23,850,121 TPT1P7, STK31
    nsv5908855copy number variation1nstd209human GRCh38 chr7: 23,813,001-23,813,088 , GRCh37.p13 chr7: 23,852,620-23,852,707 STK31
    nsv5908682copy number variation1nstd209human GRCh38 chr7: 23,729,555-23,729,639 , GRCh37.p13 chr7: 23,769,174-23,769,258 STK31
    nsv5693785mobile element insertion2nstd211human GRCh38 chr7: 23,818,629-23,818,629 , GRCh37.p13 chr7: 23,858,248-23,858,248 STK31
    nsv5693290mobile element insertion1nstd211human GRCh38 chr7: 23,728,100-23,728,100 , GRCh37.p13 chr7: 23,767,719-23,767,719 STK31
    nsv5691450mobile element insertion2nstd211human GRCh38 chr7: 23,809,181-23,809,181 , GRCh37.p13 chr7: 23,848,800-23,848,800 STK31
    nsv5691121mobile element insertion1nstd211human GRCh38 chr7: 23,789,486-23,789,486 , GRCh37.p13 chr7: 23,829,105-23,829,105 STK31
    nsv5683772mobile element insertion1nstd211human GRCh38 chr7: 23,751,844-23,751,844 , GRCh37.p13 chr7: 23,791,463-23,791,463 STK31
    nsv5637805insertion1nstd207human GRCh38 chr7: 23,809,167-23,809,167 , GRCh37.p13 chr7: 23,848,786-23,848,786 STK31
    nsv5629187insertion1nstd207human GRCh38 chr7: 23,729,555-23,729,555 , GRCh37.p13 chr7: 23,769,174-23,769,174 STK31
    nsv5577780copy number variation1nstd207human GRCh38 chr7: 23,810,422-23,810,502 , GRCh37.p13 chr7: 23,850,041-23,850,121 STK31, TPT1P7
    nsv5561272sequence alteration1nstd206human GRCh38 chr7: 23,740,705-23,744,875 , GRCh37.p13 chr7: 23,780,324-23,784,494 STK31
    nsv5558540inversion1nstd206human GRCh38 chr7: 23,775,249-23,799,124 , GRCh37.p13 chr7: 23,814,868-23,838,743 STK31
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5548683insertion1nstd206human GRCh38 chr7: 23,785,704-23,785,714 , GRCh37.p13 chr7: 23,825,323-23,825,333 STK31
    nsv5548434insertion1nstd206human GRCh38 chr7: 23,740,147-23,740,159 , GRCh37.p13 chr7: 23,779,766-23,779,778 STK31
    nsv5540543insertion1nstd206human GRCh38 chr7: 23,743,134-23,743,174 , GRCh37.p13 chr7: 23,782,753-23,782,793 STK31
    nsv5475394copy number variation1nstd206human GRCh38 chr7: 23,782,352-23,782,455 , GRCh37.p13 chr7: 23,821,971-23,822,074 STK31
    nsv5474964copy number variation1nstd206human GRCh38 chr7: 23,740,700-23,744,913 , GRCh37.p13 chr7: 23,780,319-23,784,532 STK31
    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