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Items: 1 to 20 of 445

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7067441inversion1nstd229human GRCh38 chr8: 27,653,428-27,653,617 , GRCh37.p13 chr8: 27,510,945-27,511,134 SCARA3
    nsv7061563inversion1nstd229human GRCh38 chr8: 27,492,341-29,312,113 , GRCh37.p13 chr8: 27,349,858-29,169,630 LOC100130612, HMBOX1, 37 more genes
    nsv6856585copy number variation1nstd229human GRCh38 chr8: 27,670,718-27,675,604 , GRCh37.p13 chr8: 27,528,235-27,533,121 SCARA3
    nsv6855109copy number variation1nstd229human GRCh38 chr8: 27,697,401-27,708,900 , GRCh37.p13 chr8: 27,554,918-27,566,417 MIR3622A, MIR3622B, 1 more genes
    nsv6849231copy number variation1nstd229human GRCh38 chr8: 27,600,061-27,761,033 , GRCh37.p13 chr8: 27,457,578-27,618,550 MIR6843, CCDC25, 6 more genes
    nsv6848547copy number variation1nstd229human GRCh38 chr8: 27,727,327-27,727,474 , GRCh37.p13 chr8: 27,584,844-27,584,991 SCARA3
    nsv6847529copy number variation1nstd229human GRCh38 chr8: 27,670,701-27,675,600 , GRCh37.p13 chr8: 27,528,218-27,533,117 SCARA3
    nsv6846389copy number variation1nstd229human GRCh38 chr8: 27,685,159-27,688,813 , GRCh37.p13 chr8: 27,542,676-27,546,330 SCARA3
    nsv6840116copy number variation1nstd229human GRCh38 chr8: 27,719,764-27,728,307 , GRCh37.p13 chr8: 27,577,281-27,585,824 SCARA3
    nsv6840098copy number variation1nstd229human GRCh38 chr8: 27,644,144-27,648,643 , GRCh37.p13 chr8: 27,501,661-27,506,160 SCARA3
    nsv6840042copy number variation1nstd229human GRCh38 chr8: 27,700,271-27,727,097 , GRCh37.p13 chr8: 27,557,788-27,584,614 SCARA3, MIR3622B, 1 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
    nsv6636640copy number variation1nstd102humanUncertain significance GRCh37 chr8: 27,064,033-28,832,392 , GRCh38.p12 chr8: 27,206,516-28,974,875 ZNF395, PNOC, 39 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6565952inversion1nstd223human GRCh38 chr8: 27,726,570-27,727,028 , GRCh37.p13 chr8: 27,584,087-27,584,545 SCARA3
    nsv6565031inversion1nstd223human GRCh38 chr8: 22,900,235-30,247,902 , GRCh37.p13 chr8: 22,757,748-30,105,418 LOC105379349, MIR6876, 140 more genes
    nsv6562502inversion1nstd223human GRCh38 chr8: 27,710,148-27,711,091 , GRCh37.p13 chr8: 27,567,665-27,568,608 SCARA3
    nsv6430917copy number variation1nstd223human GRCh38 chr8: 27,670,711-27,675,596 , GRCh37.p13 chr8: 27,528,228-27,533,113 SCARA3
    nsv6421036copy number variation1nstd223human GRCh38 chr8: 27,720,633-27,720,979 , GRCh37.p13 chr8: 27,578,150-27,578,496 SCARA3
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