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 146

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7075094inversion1nstd229human GRCh38 chr16: 67,913,190-69,541,641 , GRCh37.p13 chr16: 67,947,093-69,575,544 PSMB10, COG8, 52 more genes
    nsv7075084inversion1nstd229human GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387 MIR1538, LINC02136, 187 more genes
    nsv7058675inversion1nstd229human GRCh38 chr16: 67,667,666-75,720,241 , GRCh37.p13 chr16: 67,701,569-75,754,139 RNU6-898P, DPEP2, 199 more genes
    nsv6983221copy number variation1nstd229human GRCh38 chr16: 69,339,885-69,340,005 , GRCh37.p13 chr16: 69,373,788-69,373,908 COG8, NIP7
    nsv6982111copy number variation1nstd229human GRCh38 chr16: 69,320,238-69,330,852 , GRCh37.p13 chr16: 69,354,141-69,364,755 VPS4A, PDF, 1 more genes
    nsv6315469copy number variation1nstd102humanPathogenic GRCh37 chr16: 68,971,067-74,823,560 , GRCh38.p12 chr16: 68,937,164-74,789,662 ZNF19, RNU7-71P, 128 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6313976copy number variation1nstd102humanUncertain significance GRCh37 chr16: 68,850,677-69,377,553 , GRCh38.p12 chr16: 68,816,774-69,343,650 HAS3, LOC101060098, 17 more genes
    nsv6197977copy number variation1nstd214human GRCh38 chr16: 69,325,359-69,325,426 , GRCh37.p13 chr16: 69,359,262-69,359,329 VPS4A, PDF, 1 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6039066copy number variation1nstd212human GRCh38 chr16: 69,325,382-69,325,439 , GRCh37.p13 chr16: 69,359,285-69,359,342 VPS4A, PDF, 1 more genes
    nsv5939831copy number variation1nstd209human GRCh38 chr16: 69,339,885-69,340,004 , GRCh37.p13 chr16: 69,373,788-69,373,907 NIP7, COG8
    nsv5937205copy number variation1nstd209human GRCh38 chr16: 69,325,359-69,325,426 , GRCh37.p13 chr16: 69,359,262-69,359,329 VPS4A, PDF, 1 more genes
    nsv5596227copy number variation1nstd207human GRCh38 chr16: 69,325,359-69,325,426 , GRCh37.p13 chr16: 69,359,262-69,359,329 VPS4A, PDF, 1 more genes
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv5005808copy number variation1nstd200human GRCh38 chr16: 69,324,958-69,365,147 , GRCh37.p13 chr16: 69,358,861-69,399,050 NIP7, PDF, 4 more genes
    nsv4993197copy number variation1nstd200human GRCh38 chr16: 69,326,002-69,330,956 , GRCh37.p13 chr16: 69,359,905-69,364,859 PDF, VPS4A, 1 more genes
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 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