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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145322insertion1nstd232human GRCh37.p13 chr8: 86,129,729-86,129,729 , GRCh38.p12 chr8: 85,217,500-85,217,500 RBIS
    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
    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
    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
    nsv6567558inversion1nstd223human GRCh38 chr8: 85,212,905-85,213,550 , GRCh37.p13 chr8: 86,125,140-86,125,785 E2F5, RBIS
    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
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136596copy number variation1nstd213human GRCh37 chr8: 72,190,000-86,530,001 , GRCh38.p12 chr8: 71,277,765-85,617,772 ACTBP6, CA2, 173 more genes
    nsv6136080copy number variation1nstd213human GRCh37 chr8: 85,790,000-86,220,001 , GRCh38.p12 chr8: 84,877,765-85,307,772 JCHAINP1, LRRCC1, 9 more genes
    nsv5101770mobile element insertion1nstd203human GRCh38 chr8: 85,212,918-85,212,954 , GRCh37.p13 chr8: 86,125,153-86,125,189 E2F5, RBIS
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
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