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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5927816copy number variation1nstd209human GRCh38 chr16: 4,253,667-4,253,751 , GRCh37.p13 chr16: 4,303,668-4,303,752 , LINC01569
    nsv5878195copy number variation1nstd209human GRCh38 chr16: 4,250,531-4,251,567 , GRCh37.p13 chr16: 4,300,532-4,301,568 LINC01569
    nsv5530801copy number variation1nstd206human GRCh38 chr16: 4,253,667-4,253,753 , GRCh37.p13 chr16: 4,303,668-4,303,754 , LINC01569
    nsv5518601copy number variation1nstd206human GRCh38 chr16: 4,250,208-4,251,566 , GRCh37.p13 chr16: 4,300,209-4,301,567 LINC01569
    nsv5380997copy number variation2nstd102humanUncertain significance GRCh37 chr16: 3,929,813-4,387,545 , GRCh38.p12 chr16: 3,879,812-4,337,544 DBIP3, ADCY9, 8 more genes
    nsv5349435translocation1nstd200human GRCh38 chr16: 4,253,753-4,253,753 , GRCh38 chr16: 4,253,667-4,253,667 , GRCh37.p13 chr16: 4,303,668-4,303,668 , GRCh37.p13 chr16: 4,303,754-4,303,754 , LINC01569
    nsv5302947copy number variation1nstd204human GRCh37.p13 chr16: 4,209,200-4,302,549 , GRCh38.p13 chr16: 4,159,199-4,252,548 , SRL, 2 more genes
    nsv5277106copy number variation1nstd204human GRCh38.p13 chr16: 4,159,201-4,252,600 , GRCh37.p13 chr16: 4,209,202-4,302,601 , LOC105371062, 2 more genes
    nsv5008077copy number variation1nstd200human GRCh38 chr16: 4,159,207-4,252,540 , GRCh37.p13 chr16: 4,209,208-4,302,541 , SRL, 2 more genes
    nsv4866509copy number variation1nstd200human GRCh37 chr16: 4,209,208-4,302,541 , GRCh38.p12 chr16: 4,159,207-4,252,540 , LINC01569, 2 more genes
    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
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4683689copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,777,699-4,852,592 , GRCh38.p12 chr16: 3,727,698-4,802,591 UBALD1, HMOX2, 30 more genes
    nsv4683275copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,794,875-4,387,545 , GRCh38.p12 chr16: 3,744,874-4,337,544 GLIS2-AS1, LOC105371062, 8 more genes
    nsv4675826copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,651,354-4,614,965 , GRCh38.p12 chr16: 2,601,353-4,564,964 MEFV, TRR-CCT5-1, 111 more genes
    nsv4674832copy number variation1nstd102humanUncertain significance GRCh37 chr16: 4,202,558-4,299,830 , GRCh38.p12 chr16: 4,152,557-4,249,829 LOC105371062, LINC01569, 1 more genes
    nsv4667221copy number variation1nstd186human GRCh37 chr16: 4,300,522-4,301,621 , GRCh38.p12 chr16: 4,250,521-4,251,620 LINC01569
    nsv4631534copy number variation1nstd183human GRCh37 chr16: 4,166,962-4,302,948 , GRCh38.p12 chr16: 4,116,961-4,252,947 , LINC01569, 3 more genes
    nsv4623311copy number variation1nstd183human GRCh37 chr16: 4,300,522-4,301,621 , GRCh38.p12 chr16: 4,250,521-4,251,620 LINC01569
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