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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923407copy number variation1nstd209human GRCh38 chr12: 8,472,982-8,473,292 , GRCh37.p13 chr12: 8,625,578-8,625,888 CLEC6A
    nsv5598799copy number variation1nstd207human GRCh38 chr12: 8,472,982-8,473,292 , GRCh37.p13 chr12: 8,625,578-8,625,888 CLEC6A
    nsv5509226copy number variation1nstd206human GRCh38 chr12: 8,457,794-8,457,878 , GRCh37.p13 chr12: 8,610,390-8,610,474 CLEC6A
    nsv5505302copy number variation1nstd206human GRCh38 chr12: 8,472,996-8,473,293 , GRCh37.p13 chr12: 8,625,592-8,625,889 CLEC6A
    nsv5501770copy number variation1nstd206human GRCh38 chr12: 8,478,344-8,478,569 , GRCh37.p13 chr12: 8,630,940-8,631,165 CLEC6A
    nsv5498437copy number variation1nstd206human GRCh38 chr12: 8,454,032-8,454,109 , GRCh37.p13 chr12: 8,606,628-8,606,705 CLEC6A
    nsv5383977mobile element deletion2nstd186human GRCh37 chr12: 8,625,592-8,625,889 , GRCh38.p12 chr12: 8,472,996-8,473,293 CLEC6A
    nsv5348561translocation1nstd200human GRCh38 chr12: 8,457,878-8,457,878 , GRCh38 chr12: 8,457,794-8,457,794 , GRCh37.p13 chr12: 8,610,474-8,610,474 , GRCh37.p13 chr12: 8,610,390-8,610,390 CLEC6A
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5277249copy number variation1nstd204human GRCh38.p13 chr12: 8,473,001-8,473,300 , GRCh37.p13 chr12: 8,625,597-8,625,896 CLEC6A
    nsv5207433mobile element deletion1nstd204human GRCh38.p13 chr12: 8,472,996-8,473,293 , GRCh37.p13 chr12: 8,625,592-8,625,889 CLEC6A
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4974311copy number variation1nstd200human GRCh38 chr12: 8,295,898-8,571,996 , GRCh37.p13 chr12: 8,448,494-8,724,592 SUPT4H1P2, RPL15P17, 14 more genes
    nsv4974308copy number variation1nstd200human GRCh38 chr12: 8,126,743-8,525,672 , GRCh37.p13 chr12: 8,279,339-8,678,268 LINC00937, CLEC4D, 23 more genes
    nsv4899746mobile element deletion1nstd200human GRCh38 chr12: 8,472,996-8,473,293 , GRCh37.p13 chr12: 8,625,592-8,625,889 CLEC6A
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4841551copy number variation1nstd200human GRCh37 chr12: 8,448,494-8,724,592 , GRCh38.p12 chr12: 8,295,898-8,571,996 SNRPCP7, CLEC4E, 14 more genes
    nsv4775030mobile element deletion1nstd200human GRCh37 chr12: 8,625,592-8,625,889 , GRCh38.p12 chr12: 8,472,996-8,473,293 CLEC6A
    nsv4747396copy number variation1nstd199human GRCh37 chr12: 8,625,586-8,625,897 , GRCh38.p12 chr12: 8,472,990-8,473,301 CLEC6A
    nsv4713758copy number variation3nstd195human GRCh37 chr12: 8,625,578-8,625,579 , GRCh38.p12 chr12: 8,472,982-8,472,983 CLEC6A
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