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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098039copy number variation1nstd102humanUncertain significance GRCh37 chr8: 86,053,597-87,755,855 , GRCh38.p12 chr8: 85,141,362-86,743,627 UBE2Q2P10, LOC107986954, 40 more genes
    nsv7075262inversion1nstd229human GRCh38 chr8: 83,096,825-86,720,422 , GRCh37.p13 chr8: 84,009,060-87,732,650 REXO1L1P, LOC100422614, 54 more genes
    nsv7072230inversion1nstd229human GRCh38 chr8: 82,484,343-86,070,164 , GRCh37.p13 chr8: 83,396,578-87,082,393 CA2, LOC100533622, 44 more genes
    nsv7061833inversion1nstd229human GRCh38 chr8: 85,226,325-85,583,275 , GRCh37.p13 chr8: 86,138,554-86,495,504 CA2, LOC105375936, 5 more genes
    nsv6856034copy number variation1nstd229human GRCh38 chr8: 84,505,907-85,477,334 , GRCh37.p13 chr8: 85,418,142-86,389,563 LOC100422614, LOC105375933, 16 more genes
    nsv6854075copy number variation1nstd229human GRCh38 chr8: 85,294,901-85,463,000 , GRCh37.p13 chr8: 86,207,130-86,375,229 CA3, CA2, 2 more genes
    nsv6852994copy number variation1nstd229human GRCh38 chr8: 85,443,399-85,446,517 , GRCh37.p13 chr8: 86,355,628-86,358,746 CA3-AS1, CA3
    nsv6844603copy number variation1nstd229human GRCh38 chr8: 85,269,497-85,444,161 , GRCh37.p13 chr8: 86,181,726-86,356,390 CA1, CA3-AS1, 2 more genes
    nsv6843742copy number variation1nstd229human GRCh38 chr8: 85,309,474-85,564,390 , GRCh37.p13 chr8: 86,221,703-86,476,619 CA2, CA3, 3 more genes
    nsv6840017copy number variation1nstd229human GRCh38 chr8: 85,099,696-85,541,973 , GRCh37.p13 chr8: 86,011,931-86,454,202 RBIS, CA2, 10 more genes
    nsv6637670copy number variation1nstd102humanUncertain significance GRCh37 chr8: 83,705,217-86,441,492 , GRCh38.p12 chr8: 82,792,982-85,529,263 CA13, LOC100420845, 24 more genes
    nsv6637274copy number variation1nstd102humanUncertain significance GRCh37 chr8: 86,326,757-86,844,401 , GRCh38.p12 chr8: 85,414,528-85,832,172 REXO1L2P, REXO1L11P, 15 more genes
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6568682inversion1nstd223human GRCh38 chr8: 85,226,325-85,583,279 , GRCh37.p13 chr8: 86,138,554-86,495,508 CA1, CA2, 5 more genes
    nsv6423118copy number variation1nstd223human GRCh38 chr8: 85,437,301-85,475,500 , GRCh37.p13 chr8: 86,349,530-86,387,729 CA3-AS1, CA2, 1 more genes
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6315163copy number variation1nstd102humanPathogenic GRCh37 chr8: 75,904,944-87,097,083 , GRCh38.p12 chr8: 74,992,709-86,084,854 ZNF704, RN7SL107P, 137 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6313579copy number variation1nstd102humanPathogenic GRCh37 chr8: 77,906,471-88,917,707 , GRCh38.p12 chr8: 76,994,235-87,905,479 LOC105375915, LOC105375918, 143 more genes
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