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Items: 1 to 20 of 306

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145420insertion1nstd232human GRCh37.p13 chr6: 160,656,526-160,656,526 , GRCh38.p12 chr6: 160,235,494-160,235,494 SLC22A2
    nsv7145402insertion1nstd232human GRCh37.p13 chr6: 160,656,527-160,656,527 , GRCh38.p12 chr6: 160,235,495-160,235,495 SLC22A2
    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
    nsv7048862inversion1nstd229human GRCh38 chr6: 160,230,887-160,238,116 , GRCh37.p13 chr6: 160,651,919-160,659,148 SLC22A2
    nsv6817130copy number variation1nstd229human GRCh38 chr6: 160,254,935-160,255,335 , GRCh37.p13 chr6: 160,675,967-160,676,367 SLC22A2
    nsv6816917copy number variation1nstd229human GRCh38 chr6: 160,206,718-160,217,065 , GRCh37.p13 chr6: 160,627,750-160,638,097 SLC22A2
    nsv6815761copy number variation1nstd229human GRCh38 chr6: 160,205,601-160,217,100 , GRCh37.p13 chr6: 160,626,633-160,638,132 SLC22A2
    nsv6814831copy number variation1nstd229human GRCh38 chr6: 160,228,735-160,233,926 , GRCh37.p13 chr6: 160,649,767-160,654,958 SLC22A2
    nsv6813842copy number variation1nstd229human GRCh38 chr6: 160,247,202-160,247,382 , GRCh37.p13 chr6: 160,668,234-160,668,414 SLC22A2
    nsv6808132copy number variation1nstd229human GRCh38 chr6: 160,227,601-160,233,900 , GRCh37.p13 chr6: 160,648,633-160,654,932 SLC22A2
    nsv6806122copy number variation1nstd229human GRCh38 chr6: 160,228,501-160,233,900 , GRCh37.p13 chr6: 160,649,533-160,654,932 SLC22A2
    nsv6804825copy number variation1nstd229human GRCh38 chr6: 160,207,501-160,217,000 , GRCh37.p13 chr6: 160,628,533-160,638,032 SLC22A2
    nsv6803173copy number variation1nstd229human GRCh38 chr6: 160,038,454-160,226,649 , GRCh37.p13 chr6: 160,459,486-160,647,681 CHP1P2, IGF2R, 3 more genes
    nsv6803009copy number variation1nstd229human GRCh38 chr6: 160,228,701-160,232,900 , GRCh37.p13 chr6: 160,649,733-160,653,932 SLC22A2
    nsv6802999copy number variation1nstd229human GRCh38 chr6: 160,011,914-160,955,470 , GRCh37.p13 chr6: 160,432,946-161,376,502 LOC102724087, LPAL2, 12 more genes
    nsv6801656copy number variation1nstd229human GRCh38 chr6: 160,202,901-160,257,900 , GRCh37.p13 chr6: 160,623,933-160,678,932 SLC22A2
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