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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095031copy number variation2nstd102humanPathogenic GRCh37 chr16: 56,226,148-58,768,132 , GRCh38.p12 chr16: 56,192,236-58,734,228 MT1B, LOC105371293, 92 more genes
    nsv7094589copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,016,057-58,768,132 , GRCh38.p12 chr16: 56,982,145-58,734,228 SLC38A7, SETD6, 58 more genes
    nsv6986991copy number variation1nstd229human GRCh38 chr16: 57,059,649-57,664,041 , GRCh37.p13 chr16: 57,093,561-57,697,953 CPNE2, TRL-CAG2-1, 21 more genes
    nsv6983078copy number variation1nstd229human GRCh38 chr16: 57,384,879-57,389,972 , GRCh37.p13 chr16: 57,418,791-57,423,884 CX3CL1
    nsv6980101copy number variation1nstd229human GRCh38 chr16: 57,380,001-57,392,000 , GRCh37.p13 chr16: 57,413,913-57,425,912 CX3CL1
    nsv6978535copy number variation1nstd229human GRCh38 chr16: 57,188,715-57,538,791 , GRCh37.p13 chr16: 57,222,627-57,572,703 CX3CL1, ARL2BP, 13 more genes
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6512489copy number variation1nstd223human GRCh38 chr16: 57,384,879-57,389,968 , GRCh37.p13 chr16: 57,418,791-57,423,880 CX3CL1
    nsv6511329copy number variation1nstd223human GRCh38 chr16: 57,369,253-57,379,803 , GRCh37.p13 chr16: 57,403,165-57,413,715 CX3CL1
    nsv6315060copy number variation1nstd102humanPathogenic GRCh38 chr16: 53,818,483-57,631,312 , GRCh37.p13 chr16: 53,852,395-57,665,224 LOC105371283, MT1A, 91 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
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5531313copy number variation1nstd206human GRCh38 chr16: 57,369,294-57,370,868 , GRCh37.p13 chr16: 57,403,206-57,404,780 CX3CL1
    nsv5301175copy number variation1nstd204human GRCh38.p13 chr16: 56,771,413-57,511,371 , GRCh37.p13 chr16: 56,805,325-57,545,283 , PLLP, 24 more genes
    nsv5276145copy number variation1nstd204human GRCh38.p13 chr16: 57,381,395-57,382,394 , GRCh37.p13 chr16: 57,415,307-57,416,306 CX3CL1
    nsv5269564copy number variation1nstd204human GRCh38.p13 chr16: 57,352,392-57,430,089 , GRCh37.p13 chr16: 57,386,304-57,464,001 CX3CL1, CIAPIN1, 2 more genes
    nsv5263209copy number variation1nstd204human GRCh38.p13 chr16: 56,771,401-57,423,100 , GRCh37.p13 chr16: 56,805,313-57,457,012 , NUP93, 19 more genes
    nsv5008395copy number variation1nstd200human GRCh38 chr16: 57,384,879-57,389,968 , GRCh37.p13 chr16: 57,418,791-57,423,880 CX3CL1
    nsv5008394copy number variation1nstd200human GRCh38 chr16: 57,369,256-57,379,803 , GRCh37.p13 chr16: 57,403,168-57,413,715 CX3CL1
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