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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6637554copy number variation1nstd102humanUncertain significance GRCh37 chr16: 77,231,747-77,285,850 , GRCh38.p12 chr16: 77,197,850-77,251,953 MON1B, VN2R10P, 1 more genes
    nsv3910429copy number variation1nstd102humanUncertain significance GRCh37 chr16: 76,714,549-77,233,646 , NCBI36 chr16: 75,272,050-75,791,147 , GRCh38 chr16: 76,680,652-77,199,749 MON1B, LOC100128497, 3 more genes
    nsv3890040copy number variation1nstd102humanUncertain significance GRCh37 chr16: 77,002,833-77,338,842 , GRCh38.p12 chr16: 76,968,936-77,304,945 MON1B, SYCE1L, 2 more genes
    nsv5380785copy number variation1nstd102humanUncertain significance GRCh37 chr16: 77,225,119-77,401,620 , GRCh38.p12 chr16: 77,191,222-77,367,723 MON1B, ADAMTS18, 2 more genes
    nsv3921095copy number variation1nstd102humanPathogenic NCBI36 chr16: 69,005,977-83,499,227 , GRCh38 chr16: 70,414,573-84,908,120 , GRCh37 chr16: 70,448,476-84,941,726 MON1B, NECAB2, 219 more genes
    nsv3918168copy number variation1nstd102humanPathogenic NCBI36 chr16: 71,640,867-81,167,432 , GRCh38 chr16: 73,049,467-82,576,326 , GRCh37 chr16: 73,083,366-82,609,931 MON1B, BCAR1, 125 more genes
    nsv3909917copy number variation1nstd102humanPathogenic GRCh37 chr16: 75,575,400-79,188,037 , GRCh38 chr16: 75,541,502-79,154,140 , NCBI36 chr16: 74,132,901-77,745,538 MON1B, LOC100131126, 40 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 MON1B, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 MON1B, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 MON1B, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 MON1B, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 MON1B, FTLP14, 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 MON1B, LOC105371237, 985 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 MON1B, ATMIN, 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 MON1B, CFAP69P1, 716 more genes
    nsv3891306copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261 MON1B, LOC107984894, 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 MON1B, ATP5F1AP3, 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 MON1B, LOC105376772, 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 MON1B, MC1R, 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 MON1B, LOC654780, 385 more genes
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