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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062345inversion1nstd229human GRCh38 chr16: 52,010,566-52,336,554 , GRCh37.p13 chr16: 52,044,478-52,370,466 LOC107983961, LINC02911, 5 more genes
    nsv6997437copy number variation1nstd229human GRCh38 chr16: 52,030,790-52,030,951 , GRCh37.p13 chr16: 52,064,702-52,064,863 LINC02911
    nsv6991536copy number variation1nstd229human GRCh38 chr16: 52,073,491-52,075,932 , GRCh37.p13 chr16: 52,107,403-52,109,844 LINC02911
    nsv6989038copy number variation1nstd229human GRCh38 chr16: 52,043,611-52,082,371 , GRCh37.p13 chr16: 52,077,523-52,116,283 LINC02911, LINC00919
    nsv6980964copy number variation1nstd229human GRCh38 chr16: 52,056,259-52,061,522 , GRCh37.p13 chr16: 52,090,171-52,095,434 LINC02911
    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
    nsv6514746copy number variation1nstd223human GRCh38 chr16: 52,049,790-52,050,465 , GRCh37.p13 chr16: 52,083,702-52,084,377 LINC02911
    nsv6509653copy number variation1nstd223human GRCh38 chr16: 52,064,851-52,065,296 , GRCh37.p13 chr16: 52,098,763-52,099,208 LINC02911
    nsv6508646copy number variation1nstd223human GRCh38 chr16: 52,020,801-52,100,400 , GRCh37.p13 chr16: 52,054,713-52,134,312 LINC02911, LINC00919, 1 more genes
    nsv6508409copy number variation1nstd223human GRCh38 chr16: 52,047,901-52,053,000 , GRCh37.p13 chr16: 52,081,813-52,086,912 LINC02911
    nsv6507435copy number variation1nstd223human GRCh38 chr16: 52,065,401-52,066,800 , GRCh37.p13 chr16: 52,099,313-52,100,712 LINC02911
    nsv6506084copy number variation1nstd223human GRCh38 chr16: 52,060,501-52,061,400 , GRCh37.p13 chr16: 52,094,413-52,095,312 LINC02911
    nsv6498914copy number variation1nstd223human GRCh38 chr16: 52,020,701-52,024,800 , GRCh37.p13 chr16: 52,054,613-52,058,712 LINC02911
    nsv6498389copy number variation1nstd223human GRCh38 chr16: 52,039,201-52,045,400 , GRCh37.p13 chr16: 52,073,113-52,079,312 LINC02911
    nsv6497796copy number variation1nstd223human GRCh38 chr16: 52,020,401-52,100,800 , GRCh37.p13 chr16: 52,054,313-52,134,712 LINC02180, LINC00919, 1 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
    nsv6275325copy number variation1nstd214human GRCh38 chr16: 52,024,932-52,024,986 , GRCh37.p13 chr16: 52,058,844-52,058,898 LINC02911
    nsv6273574copy number variation1nstd214human GRCh38 chr16: 52,024,946-52,025,002 , GRCh37.p13 chr16: 52,058,858-52,058,914 LINC02911
    nsv6273263copy number variation1nstd214human GRCh38 chr16: 52,024,925-52,024,974 , GRCh37.p13 chr16: 52,058,837-52,058,886 LINC02911
    nsv6273048copy number variation1nstd214human GRCh38 chr16: 52,024,932-52,024,992 , GRCh37.p13 chr16: 52,058,844-52,058,904 LINC02911
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