U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 135

    loading data ...

    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
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center