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Items: 1 to 20 of 7718

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3882358copy number variation1nstd102humanPathogenic GRCh38 chr6: 1,610,446-1,613,897 , GRCh37 chr6: 1,610,681-1,614,132 FOXC1
    nsv3879099copy number variation1nstd102humanPathogenic GRCh38 chr6: 1,610,426-1,612,841 , GRCh37.p13 chr6: 1,610,661-1,613,076 FOXC1
    nsv3877237copy number variation1nstd102humanPathogenic GRCh38 chr6: 1,610,445-1,612,107 , GRCh37 chr6: 1,610,680-1,612,342 FOXC1
    nsv997060copy number variation1nstd45humanPathogenic GRCh38.p12 chr6: 1,610,446-1,613,897 , GRCh37 chr6: 1,610,681-1,614,132 FOXC1
    nsv3883034copy number variation1nstd102humanBenign GRCh37 chr6: 2,207,469-2,208,093 , GRCh38.p12 chr6: 2,207,235-2,207,859 GMDS
    nsv3889911copy number variation1nstd102humanBenign GRCh37 chr6: 2,207,469-2,208,008 , GRCh38.p12 chr6: 2,207,235-2,207,774 GMDS
    nsv3910310copy number variation1nstd102humanUncertain significance GRCh37 chr6: 1,744,238-2,006,788 , GRCh38 chr6: 1,744,004-2,006,554 , NCBI36 chr6: 1,689,237-1,951,787 GMDS
    nsv4455720copy number variation1nstd102humanUncertain significance GRCh37 chr6: 1,910,715-2,150,669 , GRCh38.p12 chr6: 1,910,481-2,150,435 GMDS
    nsv4674961copy number variation1nstd102humanUncertain significance GRCh37 chr6: 1,970,407-2,093,302 , GRCh38.p12 chr6: 1,970,173-2,093,068 GMDS
    nsv3886705copy number variation1nstd102humanUncertain significance GRCh37 chr6: 1,875,823-1,964,471 , GRCh38.p12 chr6: 1,875,589-1,964,237 GMDS
    nsv4456285copy number variation1nstd102humanUncertain significance GRCh37 chr6: 2,113,808-2,188,830 , GRCh38.p12 chr6: 2,113,574-2,188,596 GMDS
    nsv4675879copy number variation1nstd102humanUncertain significance GRCh37 chr6: 1,949,490-1,999,263 , GRCh38.p12 chr6: 1,949,256-1,999,029 GMDS
    nsv869043copy number variation1nstd37humanUncertain significance NCBI36 chr6: 1,689,237-1,951,787 , GRCh37.p13 chr6: 1,744,238-2,006,788 , GRCh38.p12 chr6: 1,744,004-2,006,554 GMDS
    esv4003051copy number variation1estd231human GRCh37 chr6: 1,682,791-1,683,102 , GRCh38.p12 chr6: 1,682,557-1,682,868 GMDS
    esv4003052copy number variation1estd231human GRCh37 chr6: 1,905,865-1,906,146 , GRCh38.p12 chr6: 1,905,631-1,905,912 GMDS
    esv2829853copy number variation6estd206human GRCh38.p12 chr6: 31,308,833-31,336,886 , NCBI36 chr6: 31,384,589-31,412,642 , GRCh37.p13 chr6: 31,276,610-31,304,663 , GRCh37.p13 chr6|NT_167246.1: 2,623,436-2,651,073 , GRCh37.p13 chr6|NT_167249.1: 2,610,355-2,638,382 , GRCh38.p12 chr6|NT_167249.2: 2,611,057-2,639,084 LOC112267902
    nsv4660765copy number variation1nstd186human GRCh37 chr6: 2,207,342-2,208,361 , GRCh38.p12 chr6: 2,207,108-2,208,127 GMDS
    nsv4662869copy number variation1nstd186human GRCh37 chr6: 2,207,443-2,208,325 , GRCh38.p12 chr6: 2,207,209-2,208,091 GMDS
    nsv4648015copy number variation1nstd186human GRCh37 chr6: 1,905,765-1,906,146 , GRCh38.p12 chr6: 1,905,531-1,905,912 GMDS
    nsv4655938mobile element deletion1nstd186human GRCh37 chr6: 1,682,792-1,683,102 , GRCh38.p12 chr6: 1,682,558-1,682,868 GMDS
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