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 178

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5943638copy number variation1nstd209human GRCh38 chr19: 16,676,089-16,676,296 , GRCh37.p13 chr19: 16,786,900-16,787,107 TMEM38A
    nsv5869868copy number variation1nstd209human GRCh38 chr19: 16,661,923-16,663,322 , GRCh37.p13 chr19: 16,772,734-16,774,133 TMEM38A
    nsv5659349insertion1nstd207human GRCh38 chr19: 16,677,533-16,677,533 , GRCh37.p13 chr19: 16,788,344-16,788,344 TMEM38A
    nsv5600181copy number variation1nstd207human GRCh38 chr19: 16,676,089-16,676,296 , GRCh37.p13 chr19: 16,786,900-16,787,107 TMEM38A
    nsv5548925insertion1nstd206human GRCh38 chr19: 16,677,554-16,677,584 , GRCh37.p13 chr19: 16,788,365-16,788,395 TMEM38A
    nsv5526247copy number variation1nstd206human GRCh38 chr19: 16,675,640-16,676,824 , GRCh37.p13 chr19: 16,786,451-16,787,635 TMEM38A
    nsv5524484copy number variation1nstd206human GRCh38 chr19: 16,676,092-16,676,297 , GRCh37.p13 chr19: 16,786,903-16,787,108 TMEM38A
    nsv5392003copy number variation3nstd186human GRCh37 chr19: 16,786,903-16,787,108 , GRCh38.p12 chr19: 16,676,092-16,676,297 TMEM38A
    nsv5359535translocation1nstd200human GRCh38 chr19: 16,677,970-16,677,970 , GRCh38 chr19: 16,678,051-16,678,051 , GRCh37.p13 chr19: 16,788,862-16,788,862 , GRCh37.p13 chr19: 16,788,781-16,788,781 TMEM38A
    nsv5329897translocation1nstd200human GRCh37 chr19: 16,788,862-16,788,862 , GRCh37 chr19: 16,788,781-16,788,781 , GRCh38.p12 chr19: 16,677,970-16,677,970 , GRCh38.p12 chr19: 16,678,051-16,678,051 TMEM38A
    nsv5328771translocation1nstd204human GRCh38.p13 chr19: 16,676,092-16,676,092 , GRCh38.p13 chr19: 16,676,297-16,676,297 , GRCh37.p13 chr19: 16,787,108-16,787,108 , GRCh37.p13 chr19: 16,786,903-16,786,903 TMEM38A
    nsv5321745translocation1nstd204human GRCh38.p13 chr19: 16,678,051-16,678,051 , GRCh38.p13 chr19: 16,677,970-16,677,970 , GRCh37.p13 chr19: 16,788,781-16,788,781 , GRCh37.p13 chr19: 16,788,862-16,788,862 TMEM38A
    nsv5167080mobile element insertion1nstd203human GRCh38 chr19: 16,676,297-16,676,344 , GRCh37.p13 chr19: 16,787,108-16,787,155 TMEM38A
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5014601copy number variation1nstd200human GRCh38 chr19: 16,683,705-16,686,060 , GRCh37.p13 chr19: 16,794,516-16,796,871 TMEM38A
    nsv5012101copy number variation1nstd200human GRCh38 chr19: 16,676,092-16,676,297 , GRCh37.p13 chr19: 16,786,903-16,787,108 TMEM38A
    nsv4864972copy number variation1nstd200human GRCh37 chr19: 16,794,516-16,796,871 , GRCh38.p12 chr19: 16,683,705-16,686,060 TMEM38A
    nsv4860526copy number variation1nstd200human GRCh37 chr19: 16,786,903-16,787,108 , GRCh38.p12 chr19: 16,676,092-16,676,297 TMEM38A
    nsv4729750copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947 LOC105372309, RAB8A, 269 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