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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112738copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,619-3,951,208 , GRCh38.p12 chr6: 149,619-3,950,974 LINC01600, TUBB2BP1, 66 more genes
    nsv5564350copy number variation1nstd102humanUncertain significance GRCh38 chr6: 1,611,031-1,611,082 , GRCh37 chr6: 1,611,266-1,611,317 FOXC1
    nsv4949353copy number variation1nstd200human GRCh38 chr6: 1,571,695-1,728,981 , GRCh37.p13 chr6: 1,571,930-1,729,215 , FOXC1, 4 more genes
    nsv4729595copy number variation1nstd102humanPathogenic GRCh37 chr6: 152,849-1,888,703 , GRCh38.p12 chr6: 152,849-1,888,469 LINC01622, EXOC2, 24 more genes
    nsv4729315copy number variation1nstd102humanPathogenic GRCh37 chr6: 302,183-3,290,583 , GRCh38.p12 chr6: 302,183-3,290,349 RIPK1, MARK2P18, 53 more genes
    nsv4685758copy number variation1nstd102humanPathogenic GRCh37 chr6: 1,307,929-1,856,280 , GRCh38.p12 chr6: 1,307,694-1,856,046 LOC105374883, FOXF2-DT, 12 more genes
    nsv4685738copy number variation1nstd102humanPathogenic GRCh37 chr6: 1,307,929-1,713,458 , GRCh38.p12 chr6: 1,307,694-1,713,224 LOC107986555, LINC01394, 12 more genes
    nsv4678879copy number variation1nstd189human GRCh37.p13 chr6: 1,517,705-1,701,182 , GRCh38.p12 chr6: 1,517,470-1,700,948 , FOXC1, 6 more genes
    nsv4675601copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-2,208,360 , GRCh38.p12 chr6: 156,974-2,208,126 DUSP22, LOC105374869, 24 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4372722copy number variation1nstd173human GRCh37 chr6: 860,262-1,934,189 , GRCh38.p12 chr6: 860,262-1,933,955 , LOC102723944, 19 more genes
    nsv4119820copy number variation1nstd166human GRCh37.p13 chr6: 1,157,244-1,803,232 , GRCh38.p12 chr6: 1,157,009-1,802,998 , LOC107986555, 17 more genes
    nsv4115800copy number variation1nstd166human GRCh37.p13 chr6: 1,607,425-1,610,066 , GRCh38.p12 chr6: 1,607,190-1,609,831 FOXC1, FOXCUT
    nsv3924620copy number variation1nstd102humanPathogenic NCBI36 chr6: 108,083-1,974,764 , GRCh38 chr6: 163,083-2,029,531 , GRCh37 chr6: 163,083-2,029,765 LOC105374879, MARK2P18, 24 more genes
    nsv3923261copy number variation1nstd102humanPathogenic NCBI36 chr6: 1,415,511-2,642,839 , GRCh37.p13 chr6: 1,470,512-2,697,840 , GRCh38.p12 chr6: 1,470,277-2,697,606 FOXC1, HMGN2P28, 13 more genes
    nsv3923249copy number variation1nstd102humanPathogenic NCBI36 chr6: 110,675-8,981,266 , GRCh38 chr6: 165,675-9,036,034 , GRCh37 chr6: 165,675-9,036,267 LOC100506207, LOC105374889, 148 more genes
    nsv3923206copy number variation1nstd102humanPathogenic NCBI36 chr6: 108,083-3,404,840 , GRCh38 chr6: 163,083-3,459,607 , GRCh37 chr6: 163,083-3,459,841 LOC105374883, MIR4645, 58 more genes
    nsv3922576copy number variation1nstd102humanPathogenic GRCh37 chr6: 164,633-6,284,470 , GRCh38 chr6: 164,633-6,284,237 , NCBI36 chr6: 109,633-6,229,469 GLRX3P2, CDYL, 106 more genes
    nsv3922052copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414 ECI2-DT, RNU1-11P, 268 more genes
    nsv3921535copy number variation1nstd102humanUncertain significance NCBI36 chr6: 1,310,436-1,572,812 , GRCh37 chr6: 1,365,437-1,627,813 , GRCh38 chr6: 1,365,202-1,627,578 MIR6720, LOC105374883, 9 more genes
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