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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098884copy number variation1nstd102humanPathogenic GRCh37 chr6: 82,828,591-86,578,811 , GRCh38.p12 chr6: 82,118,874-85,869,093 LOC105377879, LOC100421583, 47 more genes
    nsv7052601inversion1nstd229human GRCh38 chr6: 85,122,647-85,919,414 , GRCh37.p13 chr6: 85,832,365-86,629,132 NT5E, SNORD50A, 18 more genes
    nsv6815283copy number variation1nstd229human GRCh38 chr6: 85,616,875-85,948,172 , GRCh37.p13 chr6: 86,326,593-86,657,890 LOC100127917, PKMP3, 8 more genes
    nsv6810872copy number variation1nstd229human GRCh38 chr6: 85,657,797-85,690,974 , GRCh37.p13 chr6: 86,367,515-86,400,692 SNORD50A, SNORD50B, 2 more genes
    nsv6804416copy number variation1nstd229human GRCh38 chr6: 85,675,711-85,676,051 , GRCh37.p13 chr6: 86,385,429-86,385,769 SNORD50A, SNORD50B, 1 more genes
    nsv6791212copy number variation1nstd229human GRCh38 chr6: 77,944,413-86,852,671 , GRCh37.p13 chr6: 78,654,130-87,562,389 SH3BGRL2, LCAL1, 93 more genes
    nsv6636656copy number variation1nstd102humanUncertain significance GRCh37 chr6: 86,098,133-88,663,964 , GRCh38.p12 chr6: 85,388,415-87,954,246 LINC02535, RPL7P27, 45 more genes
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 LOC101928570, RNU4-72P, 288 more genes
    nsv6290989copy number variation1nstd102humanPathogenic GRCh37 chr6: 83,141,523-88,023,466 , GRCh38.p12 chr6: 82,431,806-87,313,748 KRT18P30, LOC107986620, 58 more genes
    nsv5689602mobile element insertion2nstd211human GRCh38 chr6: 85,676,927-85,676,927 , GRCh37.p13 chr6: 86,386,645-86,386,645 SNORD50A, SNHG5, 1 more genes
    nsv5472218copy number variation1nstd206human GRCh38 chr6: 85,675,390-85,675,686 , GRCh37.p13 chr6: 86,385,108-86,385,404 SNORD50A, SNHG5, 1 more genes
    nsv5463013copy number variation1nstd206human GRCh38 chr6: 85,675,770-85,676,112 , GRCh37.p13 chr6: 86,385,488-86,385,830 SNHG5, SNORD50B, 1 more genes
    nsv5461931copy number variation1nstd206human GRCh38 chr6: 85,675,801-85,675,857 , GRCh37.p13 chr6: 86,385,519-86,385,575 SNHG5, SNORD50B, 1 more genes
    nsv5396507mobile element insertion1nstd206human GRCh38 chr6: 85,676,927-85,676,978 , GRCh37.p13 chr6: 86,386,645-86,386,696 , SNORD50A, 2 more genes
    nsv5331692translocation1nstd200human GRCh37 chr6: 86,385,108-86,385,108 , GRCh37 chr6: 86,385,404-86,385,404 , GRCh38.p12 chr6: 85,675,390-85,675,390 , GRCh38.p12 chr6: 85,675,686-85,675,686 SNORD50A, SNHG5, 1 more genes
    nsv5100943mobile element insertion1nstd203human GRCh38 chr6: 85,676,917-85,676,927 , GRCh37.p13 chr6: 86,386,635-86,386,645 SNORD50A, SNHG5, 1 more genes
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv5037999inversion1nstd200human GRCh38 chr6: 85,122,647-85,919,417 , GRCh37.p13 chr6: 85,832,365-86,629,135 , LOC100127917, 19 more genes
    nsv4945374copy number variation1nstd200human GRCh38 chr6: 85,669,744-85,682,650 , GRCh37.p13 chr6: 86,379,462-86,392,368 , SNHG5, 2 more genes
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