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Items: 1 to 20 of 267

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143097insertion1nstd232human GRCh37.p13 chr8: 86,174,350-86,174,350 , GRCh38.p12 chr8: 85,262,121-85,262,121 CA13
    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
    nsv6856056copy number variation1nstd229human GRCh38 chr8: 85,178,022-85,312,682 , GRCh37.p13 chr8: 86,090,257-86,224,911 E2F5, LOC105375936, 2 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
    nsv6852832copy number variation1nstd229human GRCh38 chr8: 85,280,651-85,296,127 , GRCh37.p13 chr8: 86,192,880-86,208,356 CA13
    nsv6852536copy number variation1nstd229human GRCh38 chr8: 85,253,370-85,253,429 , GRCh37.p13 chr8: 86,165,599-86,165,658 CA13
    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
    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
    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
    nsv6568663inversion1nstd223human GRCh38 chr8: 85,271,986-85,272,485 , GRCh37.p13 chr8: 86,184,215-86,184,714 CA13
    nsv6563692inversion1nstd223human GRCh38 chr8: 85,253,383-85,253,977 , GRCh37.p13 chr8: 86,165,612-86,166,206 CA13
    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
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