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 72

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5314396copy number variation1nstd204human GRCh37.p13 chr16: 86,587,317-86,594,238 , GRCh38.p13 chr16: 86,553,711-86,560,632 MTHFSD, FLJ30679
    nsv5299487copy number variation1nstd204human GRCh38.p13 chr16: 86,553,674-86,561,176 , GRCh37.p13 chr16: 86,587,280-86,594,782 FLJ30679, MTHFSD
    nsv5297587copy number variation1nstd204human GRCh38.p13 chr16: 86,555,049-86,556,048 , GRCh37.p13 chr16: 86,588,655-86,589,654 FLJ30679, MTHFSD
    nsv5009999copy number variation1nstd200human GRCh38 chr16: 86,551,002-86,555,011 , GRCh37.p13 chr16: 86,584,608-86,588,617 FLJ30679, MTHFSD
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729919copy number variation1nstd102humanUncertain significance GRCh37 chr16: 86,287,540-86,718,579 , GRCh38.p12 chr16: 86,253,934-86,684,973 FENDRR, FOXC2-AS1, 10 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4674955copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,872,102-87,678,641 , GRCh38.p12 chr16: 84,838,496-87,645,035 RPL7AP63, LOC105371388, 62 more genes
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
    nsv4374540copy number variation1nstd173human GRCh37 chr16: 86,359,211-86,665,459 , GRCh38.p12 chr16: 86,325,605-86,631,853 RPL7AP63, LINC00917, 8 more genes
    nsv4373011copy number variation1nstd173human GRCh37 chr16: 85,070,511-86,960,204 , GRCh38.p12 chr16: 85,036,905-86,926,598 , LOC101928502, 46 more genes
    nsv4349253copy number variation1nstd102humanPathogenic GRCh37 chr16: 82,761,333-90,055,381 , GRCh38.p12 chr16: 82,727,728-89,988,973 RN7SL134P, CDK10, 178 more genes
    nsv4236850copy number variation1nstd166human GRCh37.p13 chr16: 86,587,800-86,594,000 , GRCh38.p12 chr16: 86,554,194-86,560,394 FLJ30679, MTHFSD
    nsv4236091copy number variation1nstd166human GRCh37.p13 chr16: 86,587,112-86,587,191 , GRCh38.p12 chr16: 86,553,506-86,553,585 MTHFSD, FLJ30679
    nsv3922890copy number variation1nstd102humanPathogenic GRCh37 chr16: 70,783,301-90,163,403 , GRCh38 chr16: 70,749,398-90,096,995 , NCBI36 chr16: 69,340,802-88,690,904 GCSH, LOC390739, 362 more genes
    nsv3922616copy number variation1nstd102humanPathogenic GRCh38 chr16: 70,514,631-90,081,985 , NCBI36 chr16: 69,106,035-88,675,894 , GRCh37 chr16: 70,548,534-90,148,393 FOXF1, RNA5SP431, 367 more genes
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 LOC105371237, IGHV3OR16-11, 985 more genes
    nsv3919844copy number variation1nstd102humanPathogenic GRCh38 chr16: 78,704,275-87,819,342 , GRCh37 chr16: 78,738,172-87,852,948 , NCBI36 chr16: 77,295,673-86,410,449 RPL10AP12, LINC01082, 146 more genes
    nsv3919817copy number variation1nstd102humanPathogenic NCBI36 chr16: 63,904,799-88,675,894 , GRCh37 chr16: 65,347,298-90,148,393 , GRCh38 chr16: 65,313,395-90,081,985 LOC105376772, WWP2, 527 more genes
    nsv3918765copy number variation1nstd102humanLikely pathogenic NCBI36 chr16: 82,579,676-88,675,894 , GRCh37 chr16: 84,022,175-90,148,393 , GRCh38 chr16: 83,988,570-90,081,985 AFG3L1P, APRT, 172 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