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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148269copy number variation1nstd102humanPathogenic GRCh38 chr8: 37,814,644-38,528,889 , GRCh37.p13 chr8: 37,672,162-38,386,407 GOT1L1, FGFR1, 20 more genes
    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
    nsv6843695copy number variation1nstd229human GRCh38 chr8: 37,938,139-37,955,670 , GRCh37.p13 chr8: 37,795,657-37,813,188 GOT1L1
    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
    nsv6561586inversion1nstd223human GRCh38 chr8: 37,933,416-37,934,854 , GRCh37.p13 chr8: 37,790,934-37,792,372 GOT1L1
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6312909copy number variation5nstd102humanUncertain significance, Pathogenic GRCh37 chr8: 37,595,441-38,961,219 , GRCh38.p12 chr8: 37,737,923-39,103,700 LSM1, BAG4, 33 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
    nsv6136672copy number variation1nstd213human GRCh37 chr8: 37,710,000-37,880,001 , GRCh38.p12 chr8: 37,852,482-38,022,483 ADRB3, RAB11FIP1, 2 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
    nsv4605167copy number variation1nstd183human GRCh37 chr8: 37,792,439-37,792,623 , GRCh38.p12 chr8: 37,934,921-37,935,105 GOT1L1
    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
    nsv4374467copy number variation1nstd173human GRCh37 chr8: 37,692,087-37,883,453 , GRCh38.p12 chr8: 37,834,569-38,025,935 BRF2, RAB11FIP1, 4 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
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