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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137133copy number variation1nstd102humanUncertain significance GRCh37 chr6: 159,006,336-170,713,678 , GRCh38.p12 chr6: 158,585,304-170,404,590 LOC101929460, GPR31, 199 more genes
    nsv7097050copy number variation2nstd102humanPathogenic GRCh37 chr6: 158,532,398-162,868,359 , GRCh38.p12 chr6: 158,111,366-162,447,327 LOC107986665, HNRNPH1P1, 64 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
    nsv6816439copy number variation1nstd229human GRCh38 chr6: 159,740,061-159,745,079 , GRCh37.p13 chr6: 160,161,093-160,166,111 WTAP, SOD2
    nsv6813969copy number variation1nstd229human GRCh38 chr6: 159,744,204-159,744,234 , GRCh37.p13 chr6: 160,165,236-160,165,266 WTAP, SOD2
    nsv6800555copy number variation1nstd229human GRCh38 chr6: 159,658,014-159,741,471 , GRCh37.p13 chr6: 160,079,046-160,162,503 WTAP, HNRNPH1P1, 2 more genes
    nsv6800228copy number variation1nstd229human GRCh38 chr6: 159,748,201-160,017,300 , GRCh37.p13 chr6: 160,169,233-160,438,332 MRPL18, MAS1, 10 more genes
    nsv6800090copy number variation1nstd229human GRCh38 chr6: 159,734,858-159,969,284 , GRCh37.p13 chr6: 160,155,890-160,390,316 PNLDC1, TCP1, 9 more genes
    nsv6634356copy number variation1nstd102humanPathogenic GRCh37 chr6: 157,318,401-165,233,548 , GRCh38.p12 chr6: 156,997,267-164,820,059 LOC105378097, LOC105378094, 103 more genes
    nsv6605539copy number variation1nstd223human GRCh38 chr6: 159,653,701-159,728,800 , GRCh37.p13 chr6: 160,074,733-160,149,832 WTAP, HNRNPH1P1, 2 more genes
    nsv6575012inversion1nstd223human GRCh38 chr6: 159,735,167-159,735,560 , GRCh37.p13 chr6: 160,156,199-160,156,592 SOD2, WTAP
    nsv6573818inversion1nstd223human GRCh38 chr6: 153,431,058-160,785,713 , GRCh37.p13 chr6: 153,752,193-161,206,745 MTRES1P1, SOD2-OT1, 106 more genes
    nsv6564527inversion1nstd223human GRCh38 chr6: 150,782,887-160,100,808 , GRCh37.p13 chr6: 151,104,023-160,521,840 RPL31P29, RPL17P24, 139 more genes
    nsv6562231inversion1nstd223human GRCh38 chr6: 150,783,018-160,100,808 , GRCh37.p13 chr6: 151,104,154-160,521,840 ARMT1, LOC102723831, 139 more genes
    nsv6558878inversion1nstd223human GRCh38 chr6: 153,428,103-160,785,918 , GRCh37.p13 chr6: 153,749,238-161,206,950 IGF2R, SOD2-OT1, 106 more genes
    nsv6315428copy number variation1nstd102humanPathogenic GRCh37 chr6: 159,121,459-170,919,482 , GRCh38.p12 chr6: 158,700,427-170,610,394 TBP, LOC105378130, 200 more genes
    nsv6313530copy number variation1nstd102humanPathogenic GRCh37 chr6: 153,207,930-164,322,346 , GRCh38.p12 chr6: 152,886,795-163,901,314 RSPH3, FBXO5, 144 more genes
    nsv6135493copy number variation1nstd213human GRCh37 chr6: 158,200,000-160,910,001 , GRCh38.p12 chr6: 157,778,968-160,488,969 ACAT2, IGF2R, 56 more genes
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