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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6817834copy number variation1nstd229human GRCh38 chr6: 105,090,057-105,142,785 , GRCh37.p13 chr6: 105,537,932-105,590,660 BVES, BVES-AS1
    nsv6811725copy number variation1nstd229human GRCh38 chr6: 105,130,441-105,133,365 , GRCh37.p13 chr6: 105,578,316-105,581,240 BVES
    nsv6806679copy number variation1nstd229human GRCh38 chr6: 105,097,868-105,108,481 , GRCh37.p13 chr6: 105,545,743-105,556,356 BVES
    nsv6804564copy number variation1nstd229human GRCh38 chr6: 105,119,978-105,120,297 , GRCh37.p13 chr6: 105,567,853-105,568,172 BVES
    nsv6801182copy number variation1nstd229human GRCh38 chr6: 105,090,325-105,179,012 , GRCh37.p13 chr6: 105,538,200-105,626,887 BVES, POPDC3, 1 more genes
    nsv6800488copy number variation1nstd229human GRCh38 chr6: 102,462,202-105,809,924 , GRCh37.p13 chr6: 102,910,077-106,257,799 LIN28B, LIN28B-AS1, 20 more genes
    nsv6798693copy number variation1nstd229human GRCh38 chr6: 104,987,891-105,102,052 , GRCh37.p13 chr6: 105,435,766-105,549,927 LIN28B, BVES, 1 more genes
    nsv6636533copy number variation1nstd102humanPathogenic GRCh37 chr6: 96,596,732-105,554,568 , GRCh38.p12 chr6: 96,148,856-105,106,693 MCHR2-AS1, ACTG1P18, 65 more genes
    nsv6636510copy number variation1nstd102humanUncertain significance GRCh37 chr6: 105,551,316-105,870,467 , GRCh38.p12 chr6: 105,103,441-105,422,592 POPDC3, PREP, 4 more genes
    nsv6636338copy number variation1nstd102humanPathogenic GRCh37 chr6: 96,946,110-106,497,526 , GRCh38.p12 chr6: 96,498,234-106,049,651 BVES-AS1, LIN28B, 74 more genes
    nsv6616244copy number variation1nstd223human GRCh38 chr6: 105,109,501-105,111,900 , GRCh37.p13 chr6: 105,557,376-105,559,775 BVES
    nsv6613420copy number variation1nstd223human GRCh38 chr6: 105,120,201-105,207,400 , GRCh37.p13 chr6: 105,568,076-105,655,275 POPDC3, BVES-AS1, 1 more genes
    nsv6605940copy number variation1nstd223human GRCh38 chr6: 105,119,978-105,120,297 , GRCh37.p13 chr6: 105,567,853-105,568,172 BVES
    nsv6566160inversion1nstd223human GRCh38 chr6: 105,123,509-105,124,138 , GRCh37.p13 chr6: 105,571,384-105,572,013 BVES
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
    nsv6313603copy number variation1nstd102humanUncertain significance GRCh37 chr6: 105,406,897-105,573,285 , GRCh38.p12 chr6: 104,959,022-105,125,410 RNU6-1106P, BVES, 1 more genes
    nsv6301677copy number variation1nstd186human GRCh37 chr6: 105,567,842-105,568,172 , GRCh38.p12 chr6: 105,119,967-105,120,297 BVES
    nsv6284504insertion1nstd214human GRCh38 chr6: 105,119,978-105,119,978 , GRCh37.p13 chr6: 105,567,853-105,567,853 BVES
    nsv6141223copy number variation1nstd206human GRCh38 chr6: 105,119,958-105,120,317 , GRCh37.p13 chr6: 105,567,833-105,568,192 BVES
    nsv6135704copy number variation1nstd213human GRCh37 chr6: 105,420,000-105,580,001 , GRCh38.p12 chr6: 104,972,125-105,132,126 BVES, LIN28B, 1 more genes
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