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Items: 1 to 20 of 289

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145442insertion1nstd232human GRCh37.p13 chr6: 161,149,367-161,149,367 , GRCh38.p12 chr6: 160,728,335-160,728,335 PLG
    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
    nsv7052471inversion1nstd229human GRCh38 chr6: 160,686,228-160,932,535 , GRCh37.p13 chr6: 161,107,260-161,353,567 LOC105378093, LOC107986665, 3 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
    nsv7044583inversion1nstd229human GRCh38 chr6: 160,701,466-160,701,767 , GRCh37.p13 chr6: 161,122,498-161,122,799 PLG
    nsv6815467copy number variation1nstd229human GRCh38 chr6: 160,728,106-160,731,031 , GRCh37.p13 chr6: 161,149,138-161,152,063 PLG
    nsv6813726copy number variation1nstd229human GRCh38 chr6: 160,741,004-160,767,075 , GRCh37.p13 chr6: 161,162,036-161,188,107 PLG
    nsv6812503copy number variation1nstd229human GRCh38 chr6: 160,723,090-160,723,142 , GRCh37.p13 chr6: 161,144,122-161,144,174 PLG
    nsv6809763copy number variation1nstd229human GRCh38 chr6: 160,704,316-160,704,521 , GRCh37.p13 chr6: 161,125,348-161,125,553 PLG
    nsv6804000copy number variation1nstd229human GRCh38 chr6: 160,306,642-161,587,374 , GRCh37.p13 chr6: 160,727,674-162,008,406 LPA, MAP3K4, 12 more genes
    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
    nsv6802316copy number variation1nstd229human GRCh38 chr6: 160,705,113-160,793,395 , GRCh37.p13 chr6: 161,126,145-161,214,427 PLG, LOC107986665
    nsv6801498copy number variation1nstd229human GRCh38 chr6: 160,710,084-160,710,830 , GRCh37.p13 chr6: 161,131,116-161,131,862 PLG
    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
    nsv6631183copy number variation1nstd224human GRCh37 chr6: 161,070,529-161,152,257 , GRCh38.p12 chr6: 160,649,497-160,731,225 PLG, LPA
    nsv6630684copy number variation1nstd224human GRCh37 chr6: 161,082,461-161,153,990 , GRCh38.p12 chr6: 160,661,429-160,732,958 PLG, LPA
    nsv6614313copy number variation1nstd223human GRCh38 chr6: 160,727,401-160,728,300 , GRCh37.p13 chr6: 161,148,433-161,149,332 PLG
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