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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5516596copy number variation1nstd206human GRCh38 chr16: 9,437,338-9,440,242 , GRCh37.p13 chr16: 9,531,195-9,534,099 LOC101927026, LINC01177
    nsv4992628copy number variation1nstd200human GRCh38 chr16: 9,437,338-9,440,242 , GRCh37.p13 chr16: 9,531,195-9,534,099 LINC01177, LOC101927026
    nsv4992627copy number variation1nstd200human GRCh38 chr16: 9,430,610-9,442,617 , GRCh37.p13 chr16: 9,524,467-9,536,474 LINC01177, LOC101927026
    nsv4850349copy number variation1nstd200human GRCh37 chr16: 9,531,195-9,534,099 , GRCh38.p12 chr16: 9,437,338-9,440,242 LOC101927026, LINC01177
    nsv4850348copy number variation1nstd200human GRCh37 chr16: 9,524,467-9,536,474 , GRCh38.p12 chr16: 9,430,610-9,442,617 LINC01177, LOC101927026
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4729614copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,899,460-10,058,650 , GRCh38.p12 chr16: 8,805,603-9,964,793 CARHSP1, PMM2, 15 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4681568copy number variation2nstd102humanUncertain significance GRCh37 chr16: 8,829,577-10,274,288 , GRCh38.p12 chr16: 8,735,720-10,180,431 LOC105371075, LOC100130283, 20 more genes
    nsv4623823copy number variation1nstd183human GRCh37 chr16: 9,531,155-9,534,050 , GRCh38.p12 chr16: 9,437,298-9,440,193 LOC101927026, LINC01177
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4350523copy number variation1nstd102humanPathogenic GRCh37 chr16: 8,839,796-9,728,670 , GRCh38.p12 chr16: 8,745,939-9,634,813 LOC105371075, RPL21P119, 15 more genes
    nsv4324333inversion1nstd166human GRCh38.p12 chr16: 9,267,619-9,594,863 , GRCh37.p13 chr16: 9,361,476-9,688,720 LINC02177, LOC101927026, 4 more genes
    nsv4246645copy number variation1nstd166human GRCh37.p13 chr16: 9,488,452-9,539,196 , GRCh38.p12 chr16: 9,394,595-9,445,339 LINC02177, LINC01195, 2 more genes
    nsv4245670copy number variation1nstd166human GRCh37.p13 chr16: 9,533,419-9,542,072 , GRCh38.p12 chr16: 9,439,562-9,448,215 LOC101927026, LINC01195, 1 more genes
    nsv4241387copy number variation1nstd166human GRCh37.p13 chr16: 9,531,195-9,534,099 , GRCh38.p12 chr16: 9,437,338-9,440,242 LINC01177, LOC101927026
    nsv3923267copy number variation1nstd102humanPathogenic GRCh37 chr16: 93,732-13,420,663 , GRCh38 chr16: 43,732-13,326,806 , NCBI36 chr16: 33,732-13,328,164 METRN, FAM234A, 413 more genes
    nsv3917929copy number variation1nstd102humanPathogenic GRCh37 chr16: 96,766-11,619,372 , GRCh38 chr16: 46,766-11,525,516 , NCBI36 chr16: 36,766-11,526,873 LOC100130283, PGP, 386 more genes
    nsv3915829copy number variation1nstd102humanPathogenic NCBI36 chr16: 656,663-15,744,462 , GRCh38 chr16: 666,662-15,743,104 , GRCh37 chr16: 716,662-15,836,961 RPL35AP34, LOC100505915, 429 more genes
    nsv3915313copy number variation1nstd102humanLikely pathogenic NCBI36 chr16: 8,995,988-9,795,103 , GRCh37 chr16: 9,088,487-9,887,602 , GRCh38 chr16: 8,994,630-9,793,745 GRIN2A, HAPSTR1, 9 more genes
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