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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5863626copy number variation1nstd209human GRCh38 chr8: 93,950,187-93,967,455 , GRCh37.p13 chr8: 94,962,415-94,979,683 RPL34P18
    nsv5117143mobile element insertion1nstd203human GRCh38 chr8: 93,956,868-93,956,872 , GRCh37.p13 chr8: 94,969,096-94,969,100 RPL34P18
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4961297copy number variation1nstd200human GRCh38 chr8: 93,940,414-93,957,625 , GRCh37.p13 chr8: 94,952,642-94,969,853 PSMA2P2, RPL34P18
    nsv4675900copy number variation1nstd102humanUncertain significance GRCh37 chr8: 94,810,526-95,397,957 , GRCh38.p12 chr8: 93,798,298-94,385,729 RPL34P18, MIR378D2, 12 more genes
    nsv4604148copy number variation1nstd183human GRCh37 chr8: 94,966,576-94,974,837 , GRCh38.p12 chr8: 93,954,348-93,962,609 RPL34P18
    nsv4489494mobile element insertion1nstd166human GRCh37.p13 chr8: 94,969,091-94,969,091 , GRCh38.p12 chr8: 93,956,863-93,956,863 RPL34P18
    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
    nsv4379230copy number variation1nstd173human GRCh37 chr8: 94,729,725-96,353,188 , GRCh38.p12 chr8: 93,717,497-95,340,960 , TMEM67, 39 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
    nsv4332062inversion1nstd166human GRCh37.p13 chr8: 70,438,609-99,073,700 , GRCh38.p12 chr8: 69,526,374-98,061,472 , FTH1P11, 375 more genes
    nsv4318515inversion1nstd166human GRCh37.p13 chr8: 75,861,320-132,789,960 , GRCh38.p12 chr8: 74,949,085-131,777,713 , ANXA13, 716 more genes
    nsv4165483copy number variation1nstd166human GRCh37.p13 chr8: 94,952,642-94,969,853 , GRCh38.p12 chr8: 93,940,414-93,957,625 PSMA2P2, RPL34P18
    nsv3966338copy number variation1nstd168human GRCh38 chr8: 93,956,837-94,020,753 , GRCh37.p13 chr8: 94,969,065-95,032,981 RPL34P18
    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
    nsv3921868copy number variation1nstd102humanPathogenic NCBI36 chr8: 93,836,936-98,873,536 , GRCh38 chr8: 92,755,532-97,792,132 , GRCh37 chr8: 93,767,760-98,804,360 MIR8084, GEM, 75 more genes
    nsv3920272copy number variation1nstd102humanPathogenic NCBI36 chr8: 94,119,579-96,749,186 , GRCh37 chr8: 94,050,403-96,680,010 , GRCh38 chr8: 93,038,175-95,667,782 PLEKHF2, INTS8, 48 more genes
    nsv3919841copy number variation1nstd102humanPathogenic GRCh38 chr8: 78,614,077-145,054,634 , GRCh37 chr8: 79,526,312-146,280,020 , NCBI36 chr8: 79,688,867-146,250,824 LY6S-AS1, LOC107984017, 911 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 MIR4662B, LOC101927845, 2104 more genes
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