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Items: 1 to 20 of 197

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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
    nsv6856754copy number variation1nstd229human GRCh38 chr8: 42,552,404-42,552,431 , GRCh37.p13 chr8: 42,407,547-42,407,574 SMIM19
    nsv6852902copy number variation1nstd229human GRCh38 chr8: 42,545,506-42,555,268 , GRCh37.p13 chr8: 42,400,649-42,410,411 SMIM19
    nsv6845712copy number variation1nstd229human GRCh38 chr8: 42,536,884-42,547,709 , GRCh37.p13 chr8: 42,392,027-42,402,852 SLC20A2, SMIM19
    nsv6844598copy number variation1nstd229human GRCh38 chr8: 42,543,907-42,554,399 , GRCh37.p13 chr8: 42,399,050-42,409,542 SMIM19
    nsv6842796copy number variation1nstd229human GRCh38 chr8: 42,545,596-42,554,194 , GRCh37.p13 chr8: 42,400,739-42,409,337 SMIM19
    nsv6637131copy number variation1nstd102humanPathogenic GRCh37 chr8: 42,303,398-43,002,481 , GRCh38.p12 chr8: 42,445,880-43,147,338 RNU1-124P, LOC105379396, 13 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6567938inversion1nstd223human GRCh38 chr8: 42,545,637-42,546,869 , GRCh37.p13 chr8: 42,400,780-42,402,012 SMIM19
    nsv6425424copy number variation1nstd223human GRCh38 chr8: 42,540,801-42,542,000 , GRCh37.p13 chr8: 42,395,944-42,397,143 SMIM19, SLC20A2
    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
    nsv6136583copy number variation1nstd213human GRCh37 chr8: 42,370,000-42,570,001 , GRCh38.p12 chr8: 42,512,482-42,714,858 CHRNB3, SLC20A2, 2 more genes
    nsv6136582copy number variation1nstd213human GRCh37 chr8: 42,320,000-42,490,001 , GRCh38.p12 chr8: 42,462,482-42,634,858 SLC20A2, SMIM19
    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
    nsv5973938inversion1nstd209human GRCh38 chr8: 41,482,982-43,307,552 , GRCh37.p13 chr8: 41,340,501-43,162,695 , ANK1, 46 more genes
    nsv5917461copy number variation1nstd209human GRCh38 chr8: 41,299,580-47,196,853 , GRCh37.p13 chr8: 41,157,099-48,108,476 , AFG3L2P1, 81 more genes
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