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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935820copy number variation1nstd209human GRCh38 chr16: 27,325,112-27,339,880 , GRCh37.p13 chr16: 27,336,433-27,351,201 IL4R
    nsv5879805copy number variation1nstd209human GRCh38 chr16: 27,325,057-27,332,545 , GRCh37.p13 chr16: 27,336,378-27,343,866 IL4R
    nsv5699305mobile element insertion1nstd211human GRCh38 chr16: 27,318,661-27,318,661 , GRCh37.p13 chr16: 27,329,982-27,329,982 IL4R
    nsv5533442copy number variation1nstd206human GRCh38 chr16: 27,325,117-27,339,881 , GRCh37.p13 chr16: 27,336,438-27,351,202 IL4R
    nsv5523610copy number variation1nstd206human GRCh38 chr16: 27,201,257-27,316,154 , GRCh37.p13 chr16: 27,212,578-27,327,475 IL4R, NSMCE1, 2 more genes
    nsv5336662translocation1nstd200human GRCh37 chr16: 27,351,202-27,351,202 , GRCh37 chr16: 27,336,438-27,336,438 , GRCh38.p12 chr16: 27,325,117-27,325,117 , GRCh38.p12 chr16: 27,339,881-27,339,881 IL4R
    nsv5306627copy number variation1nstd204human GRCh38.p13 chr16: 27,325,109-27,339,888 , GRCh37.p13 chr16: 27,336,430-27,351,209 IL4R
    nsv5275194copy number variation1nstd204human GRCh38.p13 chr16: 27,333,046-27,334,245 , GRCh37.p13 chr16: 27,344,367-27,345,566 IL4R
    nsv5273966copy number variation1nstd204human GRCh38.p13 chr16: 27,325,330-27,339,701 , GRCh37.p13 chr16: 27,336,651-27,351,022 IL4R
    nsv5266517copy number variation1nstd204human GRCh38.p13 chr16: 27,325,101-27,339,900 , GRCh37.p13 chr16: 27,336,422-27,351,221 IL4R
    nsv5003359copy number variation1nstd200human GRCh38 chr16: 27,325,117-27,339,881 , GRCh37.p13 chr16: 27,336,438-27,351,202 IL4R
    nsv4864080copy number variation1nstd200human GRCh37 chr16: 26,413,712-27,385,346 , GRCh38.p12 chr16: 26,402,391-27,374,025 KDM8, EEF1A1P38, 8 more genes
    nsv4729977copy number variation1nstd102humanUncertain significance GRCh37 chr16: 27,277,775-27,814,900 , GRCh38.p12 chr16: 27,266,454-27,803,579 IL4R, LOC100128079, 9 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
    nsv4729822copy number variation1nstd102humanUncertain significance GRCh37 chr16: 26,457,597-27,420,153 , GRCh38.p12 chr16: 26,446,276-27,408,832 LINC02195, LOC105371155, 9 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
    nsv4668961copy number variation1nstd186human GRCh37 chr16: 27,325,283-27,325,332 , GRCh38.p12 chr16: 27,313,962-27,314,011 IL4R
    nsv4667082copy number variation1nstd186human GRCh37 chr16: 27,326,624-27,350,956 , GRCh38.p12 chr16: 27,315,303-27,339,635 IL4R
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