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Items: 1 to 20 of 341

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143201insertion1nstd232human GRCh37.p13 chr6: 100,407,499-100,407,499 , GRCh38.p12 chr6: 99,959,623-99,959,623 MCHR2
    nsv7042952inversion1nstd229human GRCh38 chr6: 99,567,141-99,930,538 , GRCh37.p13 chr6: 100,015,017-100,378,414 RPS3P5, CCNC, 3 more genes
    nsv6812838copy number variation1nstd229human GRCh38 chr6: 99,916,252-99,923,840 , GRCh37.p13 chr6: 100,364,128-100,371,716 MCHR2
    nsv6812303copy number variation1nstd229human GRCh38 chr6: 99,922,222-99,929,719 , GRCh37.p13 chr6: 100,370,098-100,377,595 MCHR2
    nsv6812245copy number variation1nstd229human GRCh38 chr6: 99,971,144-100,007,344 , GRCh37.p13 chr6: 100,419,020-100,455,220 MCHR2-AS1, MCHR2
    nsv6811140copy number variation1nstd229human GRCh38 chr6: 97,373,758-103,907,621 , GRCh37.p13 chr6: 97,821,634-104,355,496 FBXL4, PRDM13, 37 more genes
    nsv6808402copy number variation1nstd229human GRCh38 chr6: 99,928,110-99,928,143 , GRCh37.p13 chr6: 100,375,986-100,376,019 MCHR2
    nsv6804300copy number variation1nstd229human GRCh38 chr6: 99,956,555-99,962,753 , GRCh37.p13 chr6: 100,404,431-100,410,629 MCHR2
    nsv6803850copy number variation1nstd229human GRCh38 chr6: 99,868,143-100,064,208 , GRCh37.p13 chr6: 100,316,019-100,512,084 MCHR2-AS1, MCHR2, 1 more genes
    nsv6801146copy number variation1nstd229human GRCh38 chr6: 99,958,150-99,958,543 , GRCh37.p13 chr6: 100,406,026-100,406,419 MCHR2
    nsv6800218copy number variation1nstd229human GRCh38 chr6: 99,899,220-99,945,068 , GRCh37.p13 chr6: 100,347,096-100,392,944 MCHR2
    nsv6636908copy number variation1nstd102humanUncertain significance GRCh37 chr6: 100,403,323-100,774,188 , GRCh38.p12 chr6: 99,955,447-100,326,312 MCHR2-AS1, PRDX2P4, 5 more genes
    nsv6636533copy number variation1nstd102humanPathogenic GRCh37 chr6: 96,596,732-105,554,568 , GRCh38.p12 chr6: 96,148,856-105,106,693 MCHR2-AS1, ACTG1P18, 65 more genes
    nsv6636338copy number variation1nstd102humanPathogenic GRCh37 chr6: 96,946,110-106,497,526 , GRCh38.p12 chr6: 96,498,234-106,049,651 BVES-AS1, LIN28B, 74 more genes
    nsv6630468copy number variation1nstd224human GRCh37 chr6: 100,277,840-100,642,867 , GRCh38.p12 chr6: 99,829,964-100,194,991 MCHR2, PRDX2P4, 5 more genes
    nsv6617988copy number variation1nstd223human GRCh38 chr6: 99,991,301-99,996,200 , GRCh37.p13 chr6: 100,439,177-100,444,076 MCHR2-AS1, MCHR2
    nsv6617352copy number variation1nstd223human GRCh38 chr6: 99,965,486-99,978,800 , GRCh37.p13 chr6: 100,413,362-100,426,676 MCHR2
    nsv6612799copy number variation1nstd223human GRCh38 chr6: 99,922,583-99,936,394 , GRCh37.p13 chr6: 100,370,459-100,384,270 MCHR2
    nsv6610948copy number variation1nstd223human GRCh38 chr6: 99,837,134-100,086,836 , GRCh37.p13 chr6: 100,285,010-100,534,712 NPM1P38, MCHR2-AS1, 1 more genes
    nsv6610587copy number variation1nstd223human GRCh38 chr6: 99,956,551-99,962,758 , GRCh37.p13 chr6: 100,404,427-100,410,634 MCHR2
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