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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv7097903copy number variation1nstd102humanUncertain significance GRCh37 chr8: 41,518,984-42,698,237 , GRCh38.p12 chr8: 41,661,466-42,843,094 DKK4, KAT6A, 22 more genes
    nsv7097662copy number variation2nstd102humanUncertain significance GRCh37 chr8: 41,518,984-43,054,712 , GRCh38.p12 chr8: 41,661,466-43,199,569 LOC101059972, IKBKB-DT, 31 more genes
    nsv7065639inversion1nstd229human GRCh38 chr8: 40,079,981-42,715,940 , GRCh37.p13 chr8: 39,937,500-42,571,083 LOC105379390, RPL17P30, 44 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6570102inversion1nstd223human GRCh38 chr8: 42,400,131-42,400,737 , GRCh37.p13 chr8: 42,257,649-42,258,255 VDAC3
    nsv6435323copy number variation1nstd223human GRCh38 chr8: 42,403,431-42,407,496 , GRCh37.p13 chr8: 42,260,949-42,265,014 VDAC3
    nsv6429801copy number variation1nstd223human GRCh38 chr8: 42,386,568-42,390,521 , GRCh37.p13 chr8: 42,244,086-42,248,039 VDAC3, DKK4
    nsv6416648copy number variation1nstd223human GRCh38 chr8: 42,389,701-42,395,400 , GRCh37.p13 chr8: 42,247,219-42,252,918 DKK4, VDAC3
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6313701copy number variation1nstd102humanUncertain significance GRCh37 chr8: 42,162,574-48,757,095 , GRCh38.p12 chr8: 42,305,056-47,844,534 RNU1-124P, LOC728587, 66 more genes
    nsv6186569copy number variation1nstd214human GRCh38 chr8: 42,390,280-42,390,384 , GRCh37.p13 chr8: 42,247,798-42,247,902 VDAC3, DKK4
    nsv6136049copy number variation1nstd213human GRCh37 chr8: 42,190,000-43,790,001 , GRCh38.p12 chr8: 42,332,482-43,934,858 IKBKB, SLC20A2, 29 more genes
    nsv6136047copy number variation1nstd213human GRCh37 chr8: 41,160,000-42,320,001 , GRCh38.p12 chr8: 41,302,481-42,462,483 SLC20A2, GOLGA7, 27 more genes
    nsv5973938inversion1nstd209human GRCh38 chr8: 41,482,982-43,307,552 , GRCh37.p13 chr8: 41,340,501-43,162,695 , ANK1, 46 more genes
    nsv5926037copy number variation1nstd209human GRCh38 chr8: 42,390,280-42,390,384 , GRCh37.p13 chr8: 42,247,798-42,247,902 DKK4, VDAC3
    nsv5917461copy number variation1nstd209human GRCh38 chr8: 41,299,580-47,196,853 , GRCh37.p13 chr8: 41,157,099-48,108,476 , AFG3L2P1, 81 more genes
    nsv5492900copy number variation1nstd206human GRCh38 chr8: 42,390,280-42,390,385 , GRCh37.p13 chr8: 42,247,798-42,247,903 DKK4, VDAC3
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4967160copy number variation1nstd200human GRCh38 chr8: 42,391,528-42,391,609 , GRCh37.p13 chr8: 42,249,046-42,249,127 VDAC3, DKK4
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