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Items: 1 to 20 of 459

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148221copy number variation1nstd102humanPathogenic GRCh38 chr6: 150,905,553-158,511,926 , GRCh37.p13 chr6: 151,226,689-158,932,958 RNU6-824P, LOC105378067, 97 more genes
    nsv7142586insertion1nstd232human GRCh37.p13 chr6: 155,141,467-155,141,467 , GRCh38.p12 chr6: 154,820,333-154,820,333 SCAF8
    nsv7053202inversion1nstd229human GRCh38 chr6: 154,191,529-154,872,823 , GRCh37.p13 chr6: 154,512,663-155,193,957 MTRES1P1, OPRM1, 11 more genes
    nsv7053022inversion1nstd229human GRCh38 chr6: 153,431,159-160,785,697 , GRCh37.p13 chr6: 153,752,294-161,206,729 OPRM1, FNDC1-AS1, 106 more genes
    nsv7052273inversion1nstd229human GRCh38 chr6: 153,428,141-160,785,922 , GRCh37.p13 chr6: 153,749,276-161,206,954 LOC442272, CACYBPP3, 106 more genes
    nsv7050008inversion1nstd229human GRCh38 chr6: 153,421,054-160,785,901 , GRCh37.p13 chr6: 153,742,189-161,206,933 SLC22A2, IGF2R, 108 more genes
    nsv7040600inversion1nstd229human GRCh38 chr6: 153,683,778-158,739,378 , GRCh37.p13 chr6: 154,004,913-159,160,410 TMEM242, RPL17P24, 59 more genes
    nsv6817110copy number variation1nstd229human GRCh38 chr6: 154,783,963-154,787,359 , GRCh37.p13 chr6: 155,105,097-155,108,493 SCAF8
    nsv6815213copy number variation1nstd229human GRCh38 chr6: 154,753,516-154,767,905 , GRCh37.p13 chr6: 155,074,650-155,089,039 SCAF8
    nsv6813848copy number variation1nstd229human GRCh38 chr6: 154,525,321-154,925,321 , GRCh37.p13 chr6: 154,846,455-155,246,455 MIR1273C, LOC646274, 5 more genes
    nsv6813276copy number variation1nstd229human GRCh38 chr6: 154,796,201-154,802,000 , GRCh37.p13 chr6: 155,117,335-155,123,134 SCAF8
    nsv6812996copy number variation1nstd229human GRCh38 chr6: 154,797,110-154,801,908 , GRCh37.p13 chr6: 155,118,244-155,123,042 SCAF8
    nsv6807351copy number variation1nstd229human GRCh38 chr6: 153,918,943-154,829,570 , GRCh37.p13 chr6: 154,240,078-155,150,704 RNU6-824P, LOC105378067, 11 more genes
    nsv6806935copy number variation1nstd229human GRCh38 chr6: 154,812,844-154,813,516 , GRCh37.p13 chr6: 155,133,978-155,134,650 SCAF8
    nsv6798189copy number variation1nstd229human GRCh38 chr6: 154,294,974-156,930,933 , GRCh37.p13 chr6: 154,616,108-157,252,067 LOC105378073, LOC105378067, 28 more genes
    nsv6615148copy number variation1nstd223human GRCh38 chr6: 154,755,284-154,759,009 , GRCh37.p13 chr6: 155,076,418-155,080,143 SCAF8
    nsv6613646copy number variation1nstd223human GRCh38 chr6: 154,769,901-154,772,600 , GRCh37.p13 chr6: 155,091,035-155,093,734 SCAF8
    nsv6610504copy number variation1nstd223human GRCh38 chr6: 154,796,001-154,801,900 , GRCh37.p13 chr6: 155,117,135-155,123,034 SCAF8
    nsv6608606copy number variation1nstd223human GRCh38 chr6: 154,801,101-154,801,900 , GRCh37.p13 chr6: 155,122,235-155,123,034 SCAF8
    nsv6605012copy number variation1nstd223human GRCh38 chr6: 154,797,401-154,802,500 , GRCh37.p13 chr6: 155,118,535-155,123,634 SCAF8
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