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Items: 1 to 20 of 9405

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
    nsv6137704copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,426,622-38,787,479 , GRCh38.p12 chr9: 36,426,625-38,787,482 MELK, SLC25A51, 55 more genes
    nsv6137700copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,088,563-39,092,820 , GRCh38.p12 chr9: 36,088,566-39,092,823 SNX18P3, VN1R48P, 69 more genes
    nsv6128002insertion1nstd186human GRCh37 chrX: 1,752,846-1,752,846 , GRCh38.p12 chrX: 1,633,953-1,633,953 ASMT
    nsv6121532copy number variation1nstd186human GRCh37 chr10: 135,180,209-135,180,283 , GRCh38.p12 chr10: 133,366,705-133,366,779 ECHS1
    nsv6120919copy number variation1nstd186human GRCh37 chr12: 72,356,601-72,358,166 , GRCh38.p12 chr12: 71,962,821-71,964,386 TPH2
    nsv6117468copy number variation1nstd186human GRCh37 chrX: 1,722,246-1,722,896 , GRCh38.p12 chrX: 1,603,353-1,604,003 ASMT
    nsv6116114copy number variation1nstd186human GRCh37 chrX: 1,745,638-1,745,941 , GRCh38.p12 chrX: 1,626,745-1,627,048 ASMT
    nsv6115561copy number variation1nstd186human GRCh37 chrX: 43,669,208-43,669,515 , GRCh38.p12 chrX: 43,809,961-43,810,268 MAOB
    nsv6114784copy number variation1nstd186human GRCh37 chrX: 1,749,214-1,752,594 , GRCh38.p12 chrX: 1,630,321-1,633,701 ASMT
    nsv6114646copy number variation1nstd186human GRCh37 chrX: 1,758,539-1,761,268 , GRCh38.p12 chrX: 1,639,646-1,642,375 ASMT
    nsv6114425copy number variation1nstd186human GRCh37 chrX: 1,732,325-1,735,110 , GRCh38.p12 chrX: 1,613,432-1,616,217 ASMT
    nsv6113226copy number variation1nstd186human GRCh37 chrX: 1,722,576-1,722,911 , GRCh38.p12 chrX: 1,603,683-1,604,018 ASMT
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv6112736copy number variation1nstd102humanPathogenic GRCh37 chr10: 48,301,535-51,807,296 , GRCh38.p12 chr10: 45,999,930-49,959,916 SHLD2P3, LOC100420617, 95 more genes
    nsv6112722copy number variation1nstd102humanPathogenic GRCh37 chrX: 42,069,104-45,843,277 , GRCh38.p12 chrX: 42,209,851-45,983,842 TATDN2P1, RRM2P3, 36 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
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