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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117652copy number variation1nstd186human GRCh37 chr6: 601,262-602,397 , GRCh38.p12 chr6: 601,262-602,397 EXOC2
    nsv6112738copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,619-3,951,208 , GRCh38.p12 chr6: 149,619-3,950,974 LINC01600, TUBB2BP1, 66 more genes
    nsv5959200insertion1nstd209human GRCh38 chr6: 565,074-565,074 , GRCh37.p13 chr6: 565,074-565,074 EXOC2
    nsv5952054insertion1nstd209human GRCh38 chr6: 658,667-658,667 , GRCh37.p13 chr6: 658,667-658,667 EXOC2
    nsv5906641copy number variation1nstd209human GRCh38 chr6: 501,240-501,549 , GRCh37.p13 chr6: 501,240-501,549 EXOC2
    nsv5905752copy number variation1nstd209human GRCh38 chr6: 537,181-537,516 , GRCh37.p13 chr6: 537,181-537,516 EXOC2
    nsv5902283copy number variation1nstd209human GRCh38 chr6: 515,574-515,743 , GRCh37.p13 chr6: 515,574-515,743 EXOC2
    nsv5897345copy number variation1nstd209human GRCh38 chr6: 541,555-541,618 , GRCh37.p13 chr6: 541,555-541,618 EXOC2
    nsv5897135copy number variation1nstd209human GRCh38 chr6: 666,376-667,820 , GRCh37.p13 chr6: 666,376-667,820 MARK2P18, EXOC2
    nsv5896831copy number variation1nstd209human GRCh38 chr6: 611,071-611,140 , GRCh37.p13 chr6: 611,071-611,140 EXOC2
    nsv5895183copy number variation1nstd209human GRCh38 chr6: 589,206-589,262 , GRCh37.p13 chr6: 589,206-589,262 EXOC2
    nsv5894765copy number variation1nstd209human GRCh38 chr6: 675,519-675,679 , GRCh37.p13 chr6: 675,519-675,679 EXOC2
    nsv5894252copy number variation1nstd209human GRCh38 chr6: 604,718-604,795 , GRCh37.p13 chr6: 604,718-604,795 EXOC2
    nsv5893747copy number variation1nstd209human GRCh38 chr6: 501,145-501,374 , GRCh37.p13 chr6: 501,145-501,374 EXOC2
    nsv5893133copy number variation1nstd209human GRCh38 chr6: 675,815-675,867 , GRCh37.p13 chr6: 675,815-675,867 EXOC2
    nsv5891119copy number variation1nstd209human GRCh38 chr6: 594,969-596,530 , GRCh37.p13 chr6: 594,969-596,530 EXOC2
    nsv5890989copy number variation1nstd209human GRCh38 chr6: 501,082-501,735 , GRCh37.p13 chr6: 501,082-501,735 EXOC2
    nsv5890725copy number variation1nstd209human GRCh38 chr6: 537,379-537,490 , GRCh37.p13 chr6: 537,379-537,490 EXOC2
    nsv5889888copy number variation1nstd209human GRCh38 chr6: 481,419-483,202 , GRCh37.p13 chr6: 481,419-483,202 EXOC2
    nsv5888934copy number variation1nstd209human GRCh38 chr6: 675,533-675,854 , GRCh37.p13 chr6: 675,533-675,854 EXOC2
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