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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6113332mobile element insertion1nstd186human GRCh37 chr16: 27,258,295-27,258,346 , GRCh38.p12 chr16: 27,246,974-27,247,025 NSMCE1
    nsv5933883copy number variation1nstd209human GRCh38 chr16: 27,225,933-27,226,157 , GRCh37.p13 chr16: 27,237,254-27,237,478 NSMCE1
    nsv5703688mobile element insertion2nstd211human GRCh38 chr16: 27,246,974-27,246,974 , GRCh37.p13 chr16: 27,258,295-27,258,295 NSMCE1
    nsv5660095insertion1nstd207human GRCh38 chr16: 27,246,963-27,246,963 , GRCh37.p13 chr16: 27,258,284-27,258,284 NSMCE1
    nsv5584607copy number variation1nstd207human GRCh38 chr16: 27,228,495-27,228,550 , GRCh37.p13 chr16: 27,239,816-27,239,871 NSMCE1
    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
    nsv5520972copy number variation1nstd206human GRCh38 chr16: 27,228,400-27,231,450 , GRCh37.p13 chr16: 27,239,721-27,242,771 NSMCE1
    nsv5428447mobile element insertion1nstd206human GRCh38 chr16: 27,246,974-27,247,025 , GRCh37.p13 chr16: 27,258,295-27,258,346 NSMCE1
    nsv5156026mobile element insertion1nstd203human GRCh38 chr16: 27,246,968-27,246,974 , GRCh37.p13 chr16: 27,258,289-27,258,295 NSMCE1
    nsv5153935mobile element insertion1nstd203human GRCh38 chr16: 27,246,969-27,246,974 , GRCh37.p13 chr16: 27,258,290-27,258,295 NSMCE1
    nsv5140654mobile element insertion1nstd203human GRCh38 chr16: 27,246,963-27,246,974 , GRCh37.p13 chr16: 27,258,284-27,258,295 NSMCE1
    nsv5003355copy number variation1nstd200human GRCh38 chr16: 27,228,400-27,231,450 , GRCh37.p13 chr16: 27,239,721-27,242,771 NSMCE1
    nsv5003354copy number variation1nstd200human GRCh38 chr16: 27,225,935-27,226,160 , GRCh37.p13 chr16: 27,237,256-27,237,481 NSMCE1
    nsv5003353copy number variation1nstd200human GRCh38 chr16: 27,222,157-27,225,258 , GRCh37.p13 chr16: 27,233,478-27,236,579 KDM8, NSMCE1
    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
    nsv4716753mobile element insertion1nstd186human GRCh37 chr16: 27,258,284-27,258,284 , GRCh38.p12 chr16: 27,246,963-27,246,963 NSMCE1
    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
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