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Items: 8

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    Number of Variants: 8

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv887045copy number variation2nstd71human NCBI36 chr6: 170,620,471-170,646,007 , GRCh37.p13 chr6: 170,778,546-170,804,082 , GRCh38.p12 chr6|NT_187553.1: 206,019-231,555 , GRCh38.p12 chr6: 170,469,458-170,494,994 LOC105378157
    nsv879318copy number variation371nstd71human NCBI36 chr4: 69,085,989-69,179,871 , GRCh37.p13 chr4: 69,403,394-69,497,276 , GRCh38.p12 chr4: 68,537,676-68,631,558 LOC728807, UGT2B17, 2 more genes
    nsv908379copy number variation346nstd71human NCBI36 chr17: 41,775,690-41,922,658 , GRCh37.p13 chr17: 44,419,932-44,566,775 , GRCh38.p12 chr17: 46,342,566-46,489,976 ARL17B, NSFP1, 1 more genes
    nsv908534copy number variation3nstd71human NCBI36 chr17: 41,963,034-42,092,850 , GRCh37.p13 chr17: 44,607,718-44,737,534 , GRCh38.p12 chr17: 46,530,352-46,660,168 NSF, RN7SL199P, 3 more genes
    nsv904023copy number variation257nstd71human NCBI36 chr15: 32,487,589-32,625,184 , GRCh37.p13 chr15: 34,700,297-34,837,892 , GRCh38.p12 chr15: 34,408,096-34,545,691 LOC100422491, GOLGA8B, 5 more genes
    nsv911348copy number variation463nstd71human NCBI36 chr19: 20,386,247-20,520,617 , GRCh37.p13 chr19|NW_003571053.2: 329,860-463,224 , GRCh37.p13 chr19: 20,522,409-20,728,777 , GRCh38.p12 chr19: 20,411,600-20,545,971 BNIP3P23, LOC105372317, 4 more genes
    nsv884258copy number variation146nstd71human NCBI36 chr6: 31,388,306-31,398,785 , GRCh37.p13 chr6|NT_167249.1: 2,614,037-2,624,528 , GRCh37.p13 chr6: 31,280,327-31,290,806 , GRCh38.p12 chr6: 31,312,550-31,323,029 , GRCh38.p12 chr6|NT_167249.2: 2,614,739-2,625,230 0
    nsv912365copy number variation8nstd71human NCBI36 chr19: 58,614,327-58,702,571 , GRCh37.p13 chr19: 53,922,515-54,010,759 , GRCh38.p12 chr19: 53,419,262-53,507,505 VN1R101P, ZNF765, 9 more genes
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