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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929387copy number variation1nstd209human GRCh38 chr16: 20,698,055-24,692,430 , GRCh37.p13 chr16: 20,709,377-24,703,751 , ACSM1, 87 more genes
    nsv5714518mobile element insertion1nstd211human GRCh38 chr16: 23,092,234-23,092,234 , GRCh37.p13 chr16: 23,103,555-23,103,555 USP31
    nsv5521296copy number variation1nstd206human GRCh38 chr16: 23,149,125-23,149,181 , GRCh37.p13 chr16: 23,160,446-23,160,502 USP31
    nsv5514265copy number variation1nstd206human GRCh38 chr16: 23,147,441-23,148,268 , GRCh37.p13 chr16: 23,158,762-23,159,589 USP31
    nsv5361858translocation1nstd200human GRCh38 chr16: 23,132,273-23,132,273 , GRCh38 chr3: 113,851,177-113,851,177 , GRCh37.p13 chr16: 23,143,594-23,143,594 , GRCh37.p13 chr3: 113,570,024-113,570,024 GRAMD1C, USP31, 1 more genes
    nsv5349564translocation1nstd200human GRCh38 chr16: 23,069,040-23,069,040 , GRCh38 chr16: 23,069,098-23,069,098 , GRCh37.p13 chr16: 23,080,419-23,080,419 , GRCh37.p13 chr16: 23,080,361-23,080,361 USP31
    nsv5331869translocation1nstd200human GRCh37 chr16: 23,080,361-23,080,361 , GRCh37 chr16: 23,080,419-23,080,419 , GRCh38.p12 chr16: 23,069,040-23,069,040 , GRCh38.p12 chr16: 23,069,098-23,069,098 USP31
    nsv5186542mobile element insertion1nstd203human GRCh38 chr16: 23,077,369-23,077,386 , GRCh37.p13 chr16: 23,088,690-23,088,707 USP31
    nsv5160033mobile element insertion1nstd203human GRCh38 chr16: 23,077,369-23,077,369 , GRCh37.p13 chr16: 23,088,690-23,088,690 USP31
    nsv5158767mobile element insertion1nstd203human GRCh38 chr16: 23,135,137-23,135,147 , GRCh37.p13 chr16: 23,146,458-23,146,468 USP31
    nsv5143782mobile element insertion1nstd203human GRCh38 chr16: 23,141,742-23,141,758 , GRCh37.p13 chr16: 23,153,063-23,153,079 USP31
    nsv5003188copy number variation1nstd200human GRCh38 chr16: 23,143,735-23,144,799 , GRCh37.p13 chr16: 23,155,056-23,156,120 USP31
    nsv5003187copy number variation1nstd200human GRCh38 chr16: 23,140,373-23,140,486 , GRCh37.p13 chr16: 23,151,694-23,151,807 USP31
    nsv5003186copy number variation1nstd200human GRCh38 chr16: 23,075,245-23,078,157 , GRCh37.p13 chr16: 23,086,566-23,089,478 USP31
    nsv4994551copy number variation1nstd200human GRCh38 chr16: 23,059,285-23,106,980 , GRCh37.p13 chr16: 23,070,606-23,118,301 USP31
    nsv4850724copy number variation1nstd200human GRCh37 chr16: 23,151,694-23,151,807 , GRCh38.p12 chr16: 23,140,373-23,140,486 USP31
    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
    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
    nsv4685761copy number variation1nstd102humannot provided GRCh37 chr16: 21,312,200-29,646,379 , GRCh38.p12 chr16: 21,300,879-29,635,058 NUPR1, TNRC6A, 176 more genes
    nsv4675970copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,802-29,351,826 , GRCh38.p12 chr16: 21,565,481-29,340,505 NSMCE1, LOC105371149, 152 more genes
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