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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094836copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,293,141-5,971,108 , GRCh38.p12 chr16: 3,243,141-5,921,107 MGRN1, CORO7, 76 more genes
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv6977046copy number variation1nstd229human GRCh38 chr16: 3,445,308-3,446,647 , GRCh37.p13 chr16: 3,495,308-3,496,647 NAA60
    nsv6972145copy number variation1nstd229human GRCh38 chr16: 3,451,401-3,455,200 , GRCh37.p13 chr16: 3,501,401-3,505,200 NAA60
    nsv6968857copy number variation1nstd229human GRCh38 chr16: 3,467,353-3,471,111 , GRCh37.p13 chr16: 3,517,353-3,521,111 NAA60
    nsv6968778copy number variation1nstd229human GRCh38 chr16: 3,206,227-3,444,939 , GRCh37.p13 chr16: 3,256,227-3,494,939 MEFV, ZNF597, 18 more genes
    nsv6968645copy number variation1nstd229human GRCh38 chr16: 3,403,933-3,529,577 , GRCh37.p13 chr16: 3,453,933-3,579,577 CLUAP1, C16orf90, 5 more genes
    nsv6966554copy number variation1nstd229human GRCh38 chr16: 3,462,853-3,467,747 , GRCh37.p13 chr16: 3,512,853-3,517,747 NAA60
    nsv6962673copy number variation1nstd229human GRCh38 chr16: 3,486,783-3,487,294 , GRCh37.p13 chr16: 3,536,783-3,537,294 NAA60
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6514218copy number variation1nstd223human GRCh38 chr16: 3,469,424-3,469,614 , GRCh37.p13 chr16: 3,519,424-3,519,614 NAA60
    nsv6513433copy number variation1nstd223human GRCh38 chr16: 3,442,670-3,450,668 , GRCh37.p13 chr16: 3,492,670-3,500,668 ZNF597, NAA60
    nsv6509305copy number variation1nstd223human GRCh38 chr16: 3,452,442-3,453,180 , GRCh37.p13 chr16: 3,502,442-3,503,180 NAA60
    nsv6508168copy number variation1nstd223human GRCh38 chr16: 3,418,478-3,445,377 , GRCh37.p13 chr16: 3,468,478-3,495,377 NAA60, ZNF597
    nsv6507529copy number variation1nstd223human GRCh38 chr16: 3,455,201-3,457,000 , GRCh37.p13 chr16: 3,505,201-3,507,000 NAA60
    nsv6506064copy number variation1nstd223human GRCh38 chr16: 3,440,495-3,442,451 , GRCh37.p13 chr16: 3,490,495-3,492,451 NAA60, ZNF597
    nsv6501672copy number variation1nstd223human GRCh38 chr16: 3,442,661-3,450,686 , GRCh37.p13 chr16: 3,492,661-3,500,686 ZNF597, NAA60
    nsv6499345copy number variation1nstd223human GRCh38 chr16: 3,445,281-3,446,619 , GRCh37.p13 chr16: 3,495,281-3,496,619 NAA60
    nsv6496600copy number variation1nstd223human GRCh38 chr16: 3,446,249-3,450,514 , GRCh37.p13 chr16: 3,496,249-3,500,514 NAA60
    nsv6310074copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,293,141-3,929,917 , GRCh38.p12 chr16: 3,243,141-3,879,916 MTRNR2L4, TRAP1, 26 more genes
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