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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148156copy number variation1nstd102humanPathogenic GRCh38 chr6: 161,349,282-170,584,790 , GRCh37.p13 chr6: 161,770,314-170,893,878 LOC105378126, LOC107986550, 149 more genes
    nsv7144667copy number variation1nstd232human GRCh37.p13 chr6: 169,642,680-169,642,804 , GRCh38.p12 chr6: 169,242,585-169,242,709 THBS2
    nsv7138137copy number variation1nstd232human GRCh37.p13 chr6: 169,618,044-169,618,135 , GRCh38.p12 chr6: 169,217,949-169,218,040 THBS2, THBS2-AS1
    nsv7137133copy number variation1nstd102humanUncertain significance GRCh37 chr6: 159,006,336-170,713,678 , GRCh38.p12 chr6: 158,585,304-170,404,590 LOC101929460, GPR31, 199 more genes
    nsv7051730inversion1nstd229human GRCh38 chr6: 167,665,486-170,032,054 , GRCh37.p13 chr6: 168,066,166-170,347,278 WDR27, KIF25, 49 more genes
    nsv7045607inversion1nstd229human GRCh38 chr6: 167,962,412-169,542,840 , GRCh37.p13 chr6: 168,363,092-169,942,936 LOC105378137, LOC105378140, 30 more genes
    nsv6816986copy number variation1nstd229human GRCh38 chr6: 169,252,450-169,259,756 , GRCh37.p13 chr6: 169,652,545-169,659,851 THBS2
    nsv6816705copy number variation1nstd229human GRCh38 chr6: 168,840,097-169,398,417 , GRCh37.p13 chr6: 169,240,192-169,798,512 LINC02519, LOC105378144, 10 more genes
    nsv6813938copy number variation1nstd229human GRCh38 chr6: 169,228,728-169,228,827 , GRCh37.p13 chr6: 169,628,823-169,628,922 THBS2-AS1, THBS2
    nsv6808051copy number variation1nstd229human GRCh38 chr6: 169,219,481-169,220,402 , GRCh37.p13 chr6: 169,619,576-169,620,497 THBS2-AS1, THBS2
    nsv6806086copy number variation1nstd229human GRCh38 chr6: 169,206,809-169,265,904 , GRCh37.p13 chr6: 169,606,904-169,665,999 THBS2, THBS2-AS1
    nsv6805501copy number variation1nstd229human GRCh38 chr6: 169,240,971-169,241,033 , GRCh37.p13 chr6: 169,641,066-169,641,128 THBS2
    nsv6805150copy number variation1nstd229human GRCh38 chr6: 169,207,529-169,214,924 , GRCh37.p13 chr6: 169,607,624-169,615,019 THBS2, THBS2-AS1
    nsv6802643copy number variation1nstd229human GRCh38 chr6: 168,577,532-169,423,355 , GRCh37.p13 chr6: 168,978,212-169,823,450 LINC02519, LOC105378144, 14 more genes
    nsv6801547copy number variation1nstd229human GRCh38 chr6: 169,233,577-169,234,494 , GRCh37.p13 chr6: 169,633,672-169,634,589 THBS2, THBS2-AS1
    nsv6800880copy number variation1nstd229human GRCh38 chr6: 169,227,221-169,227,281 , GRCh37.p13 chr6: 169,627,316-169,627,376 THBS2-AS1, THBS2
    nsv6800077copy number variation1nstd229human GRCh38 chr6: 169,167,491-169,344,643 , GRCh37.p13 chr6: 169,567,586-169,744,738 LOC105378148, THBS2, 3 more genes
    nsv6798206copy number variation1nstd229human GRCh38 chr6: 169,180,800-169,420,533 , GRCh37.p13 chr6: 169,580,895-169,820,628 LOC105378148, THBS2-AS1, 4 more genes
    nsv6636689copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,181,847-170,919,482 , GRCh38.p12 chr6: 162,760,815-170,610,394 GNG5P1, LINC01558, 144 more genes
    nsv6634382copy number variation1nstd102humanPathogenic GRCh37 chr6: 168,552,894-170,919,482 , GRCh38.p12 chr6: 168,152,214-170,610,394 LOC101929460, LINC01624, 49 more genes
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