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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3916762copy number variation1nstd102humanPathogenic GRCh37 chr16: 62,213,235-67,804,317 , GRCh38 chr16: 62,179,331-67,770,414 , NCBI36 chr16: 60,770,736-66,361,818 RANBP10, TMEM208, 87 more genes
    nsv4675201copy number variation1nstd102humanPathogenic GRCh37 chr16: 65,669,673-70,180,183 , GRCh38.p12 chr16: 65,635,770-70,146,280 LOC100420066, LINC00920, 143 more genes
    nsv3910745copy number variation1nstd102humanPathogenic NCBI36 chr16: 62,902,680-66,653,415 , GRCh38 chr16: 64,311,275-68,062,011 , GRCh37 chr16: 64,345,179-68,095,914 PSMB10, TPPP3, 95 more genes
    nsv7094682copy number variation2nstd102humanPathogenic GRCh37 chr16: 65,821,800-67,208,957 , GRCh38.p12 chr16: 65,787,897-67,175,054 RNA5SP428, PHAF1, 38 more genes
    nsv3918405copy number variation1nstd102humanPathogenic GRCh38 chr16: 66,245,888-67,473,023 , NCBI36 chr16: 64,837,292-66,064,427 , GRCh37 chr16: 66,279,791-67,506,926 PLEKHG4, TMEM208, 53 more genes
    nsv3923505copy number variation1nstd102humanPathogenic NCBI36 chr16: 65,285,584-66,456,849 , GRCh37 chr16: 66,728,083-67,899,348 , GRCh38 chr16: 66,694,180-67,865,445 DYNC1LI2, CIAO2B, 56 more genes
    nsv4350223copy number variation1nstd102humanPathogenic GRCh37 chr16: 67,132,790-68,166,320 , GRCh38.p12 chr16: 67,098,887-68,132,417 CBFB, B3GNT9, 55 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 CKLF, NPIPP1, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 LOC100128079, LOC105379474, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 LINC02175, FCSK, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 PRSS53, LINC02134, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 FTLP14, ZNF785, 1868 more genes
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 LOC105371237, IGHV3OR16-11, 985 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv3915506copy number variation1nstd102humanPathogenic NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062 CFAP69P1, GAS8-AS1, 716 more genes
    nsv3891306copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261 LOC107984894, BEAN1, 613 more genes
    nsv3913913copy number variation1nstd102humanPathogenic NCBI36 chr16: 62,980,782-88,675,894 , GRCh38 chr16: 64,389,378-90,081,985 , GRCh37 chr16: 64,423,281-90,148,393 ATP5F1AP3, LOC105371414, 534 more genes
    nsv3919817copy number variation1nstd102humanPathogenic NCBI36 chr16: 63,904,799-88,675,894 , GRCh37 chr16: 65,347,298-90,148,393 , GRCh38 chr16: 65,313,395-90,081,985 LOC105376772, WWP2, 527 more genes
    nsv3910304copy number variation1nstd102humanPathogenic NCBI36 chr16: 64,102,887-88,690,904 , GRCh38 chr16: 65,511,483-90,096,995 , GRCh37 chr16: 65,545,386-90,163,403 MC1R, LOC107984856, 528 more genes
    nsv3920399copy number variation1nstd102humanPathogenic NCBI36 chr16: 61,517,334-83,176,902 , GRCh37 chr16: 62,959,833-84,619,401 , GRCh38 chr16: 62,925,929-84,585,795 LOC654780, LSM3P5, 385 more genes
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