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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095898copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,223,339-44,638,757 , GRCh38.p12 chr20: 43,594,699-46,010,118 ADA, CCN5, 99 more genes
    nsv7075825inversion1nstd229human GRCh38 chr20: 45,232,922-45,712,689 , GRCh37.p13 chr20: 43,861,563-44,341,328 PIGT, LOC105372630, 33 more genes
    nsv7062736inversion1nstd229human GRCh38 chr20: 36,955,253-45,585,462 , GRCh37.p13 chr20: 35,583,656-44,214,101 GDAP1L1, PI3, 177 more genes
    nsv7033508copy number variation1nstd229human GRCh38 chr20: 45,334,083-45,346,386 , GRCh37.p13 chr20: 43,962,723-43,975,026 SDC4
    nsv7029747copy number variation1nstd229human GRCh38 chr20: 45,335,780-45,338,660 , GRCh37.p13 chr20: 43,964,420-43,967,300 SDC4
    nsv7025682copy number variation1nstd229human GRCh38 chr20: 45,327,415-45,330,365 , GRCh37.p13 chr20: 43,956,055-43,959,005 SDC4
    nsv6600060inversion1nstd223human GRCh38 chr20: 45,326,328-45,326,559 , GRCh37.p13 chr20: 43,954,968-43,955,199 SDC4
    nsv6596116inversion1nstd223human GRCh38 chr20: 36,955,253-45,585,469 , GRCh37.p13 chr20: 35,583,656-44,214,108 LOC101929863, LOC105372620, 177 more genes
    nsv6553980copy number variation1nstd223human GRCh38 chr20: 45,316,353-45,323,691 , GRCh37.p13 chr20: 43,944,993-43,952,331 SDC4, RBPJL, 1 more genes
    nsv6551757copy number variation1nstd223human GRCh38 chr20: 45,292,251-45,325,447 , GRCh37.p13 chr20: 43,920,891-43,954,087 MATN4, SDC4, 2 more genes
    nsv6538363copy number variation1nstd223human GRCh38 chr20: 45,343,150-45,344,606 , GRCh37.p13 chr20: 43,971,790-43,973,246 SDC4
    nsv6290315copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,985,044-48,599,046 , GRCh38.p12 chr20: 44,356,404-49,982,509 PABPC1L, LOC107985401, 170 more genes
    nsv6134164copy number variation1nstd213human GRCh37 chr20: 43,170,000-44,070,001 , GRCh38.p12 chr20: 44,541,359-45,441,361 PI3, SEMG2, 35 more genes
    nsv6133816copy number variation1nstd213human GRCh37 chr20: 43,650,000-45,170,001 , GRCh38.p12 chr20: 45,021,359-46,541,362 MMP9, PI3, 76 more genes
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5563618sequence alteration1nstd206human GRCh38 chr20: 45,335,591-45,337,667 , GRCh37.p13 chr20: 43,964,231-43,966,307 SDC4
    nsv5535923insertion1nstd206human GRCh38 chr20: 45,335,592-45,335,592 , GRCh37.p13 chr20: 43,964,232-43,964,232 SDC4
    nsv5524681copy number variation1nstd206human GRCh38 chr20: 45,334,454-45,334,677 , GRCh37.p13 chr20: 43,963,094-43,963,317 SDC4
    nsv5324090inversion1nstd204human GRCh37.p13 chr20: 35,583,652-44,214,109 , GRCh38.p13 chr20: 36,955,249-45,585,470 , BPI, 180 more genes
    nsv5175403mobile element insertion1nstd203human GRCh38 chr20: 45,326,382-45,326,417 , GRCh37.p13 chr20: 43,955,022-43,955,057 SDC4
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