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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5934177copy number variation1nstd209human GRCh38 chr16: 79,606,241-79,606,614 , GRCh37.p13 chr16: 79,640,138-79,640,511 LOC101928230
    nsv5516624copy number variation1nstd206human GRCh38 chr16: 78,673,486-79,733,774 , GRCh37.p13 chr16: 78,707,383-79,767,671 MAF, WWOX, 7 more genes
    nsv5310275copy number variation1nstd204human GRCh37.p13 chr16: 78,707,359-79,767,693 , GRCh38.p13 chr16: 78,673,462-79,733,796 MAF, WWOX, 7 more genes
    nsv5295745copy number variation1nstd204human GRCh37.p13 chr16: 78,686,098-79,767,697 , GRCh38.p13 chr16: 78,652,201-79,733,800 MAF, WWOX, 7 more genes
    nsv5013443copy number variation1nstd200human GRCh38 chr16: 78,673,486-79,733,774 , GRCh37.p13 chr16: 78,707,383-79,767,671 MAF, RPS3P7, 7 more genes
    nsv5009552copy number variation1nstd200human GRCh38 chr16: 79,081,287-79,809,953 , GRCh37.p13 chr16: 79,115,184-79,843,850 MAF, WWOX, 6 more genes
    nsv4866819copy number variation1nstd200human GRCh37 chr16: 79,640,140-79,640,512 , GRCh38.p12 chr16: 79,606,243-79,606,615 LOC101928230
    nsv4866800copy number variation1nstd200human GRCh37 chr16: 79,115,184-79,843,850 , GRCh38.p12 chr16: 79,081,287-79,809,953 MAF, WWOX, 6 more genes
    nsv4864293copy number variation1nstd200human GRCh37 chr16: 78,707,383-79,767,671 , GRCh38.p12 chr16: 78,673,486-79,733,774 LOC101928230, LOC112268165, 7 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4683683copy number variation1nstd102humanPathogenic GRCh37 chr16: 79,628,337-79,633,819 , GRCh38.p12 chr16: 79,594,440-79,599,922 LOC101928230, MAF
    nsv4675759copy number variation1nstd102humanUncertain significance GRCh37 chr16: 78,426,151-81,049,683 , GRCh38.p12 chr16: 78,392,254-81,016,078 LINC01227, LOC101928230, 18 more genes
    nsv4668130copy number variation1nstd186human GRCh37 chr16: 79,632,101-79,634,700 , GRCh38.p12 chr16: 79,598,204-79,600,803 MAF, LOC101928230
    nsv4633222copy number variation1nstd183human GRCh37 chr16: 79,141,670-80,132,108 , GRCh38.p12 chr16: 79,107,773-80,098,211 MAF, WWOX, 7 more genes
    nsv4632237copy number variation1nstd183human GRCh37 chr16: 79,134,295-80,130,178 , GRCh38.p12 chr16: 79,100,398-80,096,281 LINC01229, MAF, 8 more genes
    nsv4630765copy number variation1nstd183human GRCh37 chr16: 79,632,101-79,634,700 , GRCh38.p12 chr16: 79,598,204-79,600,803 MAF, LOC101928230
    nsv4457179copy number variation1nstd102humanUncertain significance GRCh37 chr16: 79,570,137-79,636,851 , GRCh38.p12 chr16: 79,536,240-79,602,954 LOC101928230, MAF
    nsv4457074copy number variation1nstd102humanUncertain significance GRCh37 chr16: 79,254,648-84,827,672 , GRCh38.p12 chr16: 79,220,751-84,794,066 MEAK7, LOC654780, 74 more genes
    nsv4454429copy number variation1nstd102humanPathogenic GRCh37 chr16: 78,312,480-80,623,263 , GRCh38 chr16: 78,278,583-80,589,366 MAFTRR, LOC107984806, 15 more genes
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