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 236

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095026copy number variation2nstd102humanUncertain significance GRCh37 chr16: 49,525,186-51,631,253 , GRCh38.p12 chr16: 49,491,275-51,597,342 RNA5SP426, RPL34P29, 35 more genes
    nsv6992376copy number variation1nstd229human GRCh38 chr16: 50,351,831-50,351,861 , GRCh37.p13 chr16: 50,385,742-50,385,772 BRD7
    nsv6990472copy number variation1nstd229human GRCh38 chr16: 50,317,296-50,317,357 , GRCh37.p13 chr16: 50,351,207-50,351,268 BRD7, ADCY7
    nsv6989834copy number variation1nstd229human GRCh38 chr16: 50,329,498-50,329,733 , GRCh37.p13 chr16: 50,363,409-50,363,644 BRD7
    nsv6984706copy number variation1nstd229human GRCh38 chr16: 50,363,829-50,366,541 , GRCh37.p13 chr16: 50,397,740-50,400,452 BRD7
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6634436copy number variation1nstd102humanassociation GRCh37 chr16: 50,089,192-51,652,287 , GRCh38.p12 chr16: 50,055,281-51,618,376 CYLD-AS1, LOC107984892, 29 more genes
    nsv6512684copy number variation1nstd223human GRCh38 chr16: 50,365,701-50,372,400 , GRCh37.p13 chr16: 50,399,612-50,406,311 BRD7
    nsv6505953copy number variation1nstd223human GRCh38 chr16: 50,339,392-50,339,760 , GRCh37.p13 chr16: 50,373,303-50,373,671 BRD7
    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
    nsv6286859insertion1nstd214human GRCh38 chr16: 50,317,296-50,317,296 , GRCh37.p13 chr16: 50,351,207-50,351,207 BRD7, ADCY7
    nsv6145664copy number variation1nstd206human GRCh38 chr16: 50,317,296-50,317,357 , GRCh37.p13 chr16: 50,351,207-50,351,268 ADCY7, BRD7
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5651929insertion1nstd207human GRCh38 chr16: 50,317,296-50,317,296 , GRCh37.p13 chr16: 50,351,207-50,351,207 BRD7, ADCY7
    nsv5524920copy number variation1nstd206human GRCh38 chr16: 50,329,498-50,329,733 , GRCh37.p13 chr16: 50,363,409-50,363,644 BRD7
    nsv5185507mobile element insertion1nstd203human GRCh38 chr16: 50,359,350-50,359,366 , GRCh37.p13 chr16: 50,393,261-50,393,277 BRD7
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4712962translocation1nstd195human GRCh38.p12 chr16: 50,334,755-50,334,755 , GRCh37 chr16: 50,368,666-50,368,666 , GRCh37 chr3: 159,819,451-159,819,451 , GRCh38.p12 chr3: 160,101,664-160,101,664 BRD7, BRD7P2, 1 more genes
    nsv4711775translocation1nstd195human GRCh38.p12 chr16: 50,334,755-50,334,755 , GRCh37 chr16: 50,368,666-50,368,666 , GRCh37 chr3: 159,819,452-159,819,452 , GRCh38.p12 chr3: 160,101,665-160,101,665 BRD7, BRD7P2, 1 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