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 805

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137770copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,215,391-41,219,624 , GRCh38.p12 chr17: 43,063,374-43,067,607 BRCA1
    nsv6137746copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,197,820-41,277,501 , GRCh38.p12 chr17: 43,045,803-43,125,484 NBR2, RPL21P4, 1 more genes
    nsv6137745copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,197,820-41,277,287 , GRCh38.p12 chr17: 43,045,803-43,125,270 NBR2, RPL21P4, 1 more genes
    nsv6137671copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 41,251,504-41,251,866 , GRCh38 chr17: 43,099,487-43,099,849 BRCA1
    nsv5980425copy number variation1nstd102humanLikely benign GRCh37 chr17: 41,209,048-41,277,500 , GRCh38.p12 chr17: 43,057,031-43,125,483 NBR2, BRCA1, 1 more genes
    nsv5972132insertion1nstd209human GRCh38 chr17: 43,100,584-43,100,584 , GRCh37.p13 chr17: 41,252,601-41,252,601 BRCA1
    nsv5940496copy number variation1nstd209human GRCh38 chr17: 43,071,727-43,072,706 , GRCh37.p13 chr17: 41,223,744-41,224,723 BRCA1
    nsv5936308copy number variation1nstd209human GRCh38 chr17: 43,053,666-43,053,972 , GRCh37.p13 chr17: 41,205,683-41,205,989 BRCA1
    nsv5882506copy number variation1nstd209human GRCh38 chr17: 43,079,970-43,082,769 , GRCh37.p13 chr17: 41,231,987-41,234,786 RPL21P4, BRCA1
    nsv5880694copy number variation1nstd209human GRCh38 chr17: 43,118,443-43,120,333 , GRCh37.p13 chr17: 41,270,460-41,272,350 BRCA1
    nsv5877924copy number variation1nstd209human GRCh38 chr17: 43,093,297-43,094,596 , GRCh37.p13 chr17: 41,245,314-41,246,613 BRCA1
    nsv5875613copy number variation1nstd209human GRCh38 chr17: 43,071,592-43,072,724 , GRCh37.p13 chr17: 41,223,609-41,224,741 BRCA1
    nsv5870631copy number variation1nstd209human GRCh38 chr17: 43,120,634-43,121,975 , GRCh37.p13 chr17: 41,272,651-41,273,992 BRCA1
    nsv5869179copy number variation1nstd209human GRCh38 chr17: 43,091,897-43,095,646 , GRCh37.p13 chr17: 41,243,914-41,247,663 BRCA1
    nsv5674277insertion1nstd102humanPathogenic GRCh37 chr17: 41,219,671-41,219,671 , GRCh38 chr17: 43,067,654-43,067,654 BRCA1
    nsv5674262insertion1nstd102humanPathogenic GRCh37 chr17: 41,228,513-41,228,513 , GRCh38 chr17: 43,076,496-43,076,496 BRCA1
    nsv5673132copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr17: 41,249,241-41,251,921 , GRCh38.p12 chr17: 43,097,224-43,099,904 BRCA1
    nsv5673131copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 41,247,857-41,251,903 , GRCh38.p12 chr17: 43,095,840-43,099,886 BRCA1
    nsv5673130copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,234,401-41,277,500 , GRCh38.p12 chr17: 43,082,384-43,125,483 NBR2, BRCA1
    nsv5673129copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,234,401-41,249,326 , GRCh38.p12 chr17: 43,082,384-43,097,309 BRCA1
    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