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 312

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112737copy number variation1nstd102humannot provided GRCh37 chr10: 14,945,105-14,954,010 , GRCh38.p12 chr10: 14,903,106-14,912,011 DCLRE1C, SUV39H2
    nsv5866373copy number variation1nstd209human GRCh38 chr10: 14,954,048-14,956,047 , GRCh37.p13 chr10: 14,996,047-14,998,046 DCLRE1C, MEIG1
    nsv5858095copy number variation1nstd209human GRCh38 chr10: 14,945,634-14,957,297 , GRCh37.p13 chr10: 14,987,633-14,999,296 MEIG1, DCLRE1C
    nsv5848764copy number variation2nstd209human GRCh38 chr10: 14,940,259-14,945,358 , GRCh37.p13 chr10: 14,982,258-14,987,357 DCLRE1C
    nsv5697649mobile element insertion1nstd211human GRCh38 chr10: 14,925,248-14,925,248 , GRCh37.p13 chr10: 14,967,247-14,967,247 DCLRE1C
    nsv5672761copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 14,969,995-14,974,974 , GRCh38.p12 chr10: 14,927,996-14,932,975 DCLRE1C
    nsv5672760copy number variation1nstd102humanPathogenic GRCh37 chr10: 14,953,179-14,961,841 , GRCh38.p12 chr10: 14,911,180-14,919,842 DCLRE1C
    nsv5672529copy number variation1nstd102humanPathogenic GRCh37 chr10: 14,946,600-14,951,339 , GRCh38.p12 chr10: 14,904,601-14,909,340 DCLRE1C, SUV39H2
    nsv5625594insertion1nstd207human GRCh38 chr10: 14,913,058-14,913,058 , GRCh37.p13 chr10: 14,955,057-14,955,057 DCLRE1C
    nsv5597903copy number variation1nstd207human GRCh38 chr10: 14,912,807-14,912,980 , GRCh37.p13 chr10: 14,954,806-14,954,979 DCLRE1C
    nsv5585405copy number variation1nstd207human GRCh38 chr10: 14,933,455-15,015,970 , GRCh37.p13 chr10: 14,975,454-15,057,969 DCLRE1C, OR7E115P, 5 more genes
    nsv5491175copy number variation1nstd206human GRCh38 chr10: 14,951,998-15,023,291 , GRCh37.p13 chr10: 14,993,997-15,065,290 DCLRE1C, OR7E115P, 5 more genes
    nsv5489033copy number variation1nstd206human GRCh38 chr10: 14,893,160-14,895,363 , GRCh37.p13 chr10: 14,935,159-14,937,362 SUV39H2, DCLRE1C
    nsv5483255copy number variation1nstd206human GRCh38 chr10: 14,950,103-15,005,437 , GRCh37.p13 chr10: 14,992,102-15,047,436 DCLRE1C, OR7E110P, 2 more genes
    nsv5386894copy number variation1nstd186human GRCh37 chr10: 14,954,882-14,955,061 , GRCh38.p12 chr10: 14,912,883-14,913,062 DCLRE1C
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv5316310copy number variation1nstd204human GRCh38.p13 chr10: 14,940,338-14,941,339 , GRCh37.p13 chr10: 14,982,337-14,983,338 DCLRE1C
    nsv5257206copy number variation1nstd204human GRCh38.p13 chr10: 14,941,079-14,943,120 , GRCh37.p13 chr10: 14,983,078-14,985,119 DCLRE1C
    nsv5137963mobile element insertion1nstd203human GRCh38 chr10: 14,908,165-14,908,187 , GRCh37.p13 chr10: 14,950,164-14,950,186 DCLRE1C
    nsv5126059mobile element insertion1nstd203human GRCh38 chr10: 14,930,221-14,930,221 , GRCh37.p13 chr10: 14,972,220-14,972,220 DCLRE1C
    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