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Items: 1 to 20 of 155

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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
    nsv6637025copy number variation1nstd102humanPathogenic GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865 LINC02948, LOC105379354, 185 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6291079copy number variation1nstd102humanUncertain significance GRCh37 chr8: 37,544,476-37,818,465 , GRCh38.p12 chr8: 37,686,958-37,960,947 ZNF703, BRF2, 10 more genes
    nsv6137281copy number variation1nstd213human GRCh37 chr8: 37,350,000-38,410,001 , GRCh38.p12 chr8: 37,492,482-38,552,483 ADRB3, EIF4EBP1, 32 more genes
    nsv6136041copy number variation1nstd213human GRCh37 chr8: 36,710,000-37,570,001 , GRCh38.p12 chr8: 36,852,482-37,712,483 SMARCE1P4, LOC100507403, 12 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4703839copy number variation1nstd195human GRCh37 chr8: 37,323,851-37,784,501 , GRCh38.p12 chr8: 37,466,333-37,926,983 LOC101929622, LOC102723701, 14 more genes
    nsv4673233copy number variation1nstd186human GRCh37 chr8: 37,551,901-37,555,000 , GRCh38.p12 chr8: 37,694,383-37,697,482 ZNF703
    nsv4610948copy number variation1nstd183human GRCh37 chr8: 37,551,901-37,555,000 , GRCh38.p12 chr8: 37,694,383-37,697,482 ZNF703
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456199copy number variation1nstd102humanUncertain significance GRCh37 chr8: 36,094,421-43,822,214 , GRCh38.p12 chr8: 36,236,903-43,967,071 AFG3L2P1, BRF2, 136 more genes
    nsv4436744copy number variation1nstd102humanUncertain significance GRCh37 chr8: 36,486,830-37,992,515 , GRCh38.p12 chr8: 36,629,312-38,134,997 LOC105379380, LOC728024, 29 more genes
    nsv4409248copy number variation1nstd174human GRCh37 chr8: 37,551,101-37,556,800 , GRCh38.p12 chr8: 37,693,583-37,699,282 ZNF703
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv3923517copy number variation1nstd102humanPathogenic NCBI36 chr8: 36,556,779-60,694,111 , GRCh37 chr8: 36,437,621-60,531,557 , GRCh38 chr8: 36,580,103-59,618,998 LOC105379380, TPT1P8, 320 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
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