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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137729copy number variation1nstd102humanBenign GRCh37 chr4: 100,522,543-100,522,628 , GRCh38 chr4: 99,601,386-99,601,471 MTTP
    nsv6120013copy number variation1nstd186human GRCh37 chr4: 100,522,544-100,522,628 , GRCh38.p12 chr4: 99,601,387-99,601,471 MTTP
    nsv5905459copy number variation1nstd209human GRCh38 chr4: 99,562,564-99,562,859 , GRCh37.p13 chr4: 100,483,721-100,484,016 MTTP, TRMT10A
    nsv5900843copy number variation1nstd209human GRCh38 chr4: 99,601,385-99,601,470 , GRCh37.p13 chr4: 100,522,542-100,522,627 MTTP
    nsv5673643copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 100,527,895-100,542,398 , GRCh38.p12 chr4: 99,606,738-99,621,241 MTTP
    nsv5619514insertion1nstd207human GRCh38 chr4: 99,588,734-99,588,734 , GRCh37.p13 chr4: 100,509,891-100,509,891 MTTP
    nsv5612040insertion1nstd207human GRCh38 chr4: 99,588,899-99,588,899 , GRCh37.p13 chr4: 100,510,056-100,510,056 MTTP
    nsv5609943insertion1nstd207human GRCh38 chr4: 99,589,035-99,589,035 , GRCh37.p13 chr4: 100,510,192-100,510,192 MTTP
    nsv5605841insertion1nstd207human GRCh38 chr4: 99,562,564-99,562,564 , GRCh37.p13 chr4: 100,483,721-100,483,721 MTTP, TRMT10A
    nsv5578829copy number variation1nstd207human GRCh38 chr4: 99,601,385-99,601,470 , GRCh37.p13 chr4: 100,522,542-100,522,627 MTTP
    nsv5564437copy number variation1nstd102humanUncertain significance GRCh37 chr4: 100,532,469-100,544,005 , GRCh38.p12 chr4: 99,611,312-99,622,848 MTTP
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5463399copy number variation1nstd206human GRCh38 chr4: 99,611,231-99,624,969 , GRCh37.p13 chr4: 100,532,388-100,546,126 MTTP
    nsv5462335copy number variation1nstd206human GRCh38 chr4: 99,601,387-99,601,471 , GRCh37.p13 chr4: 100,522,544-100,522,628 MTTP
    nsv5461851copy number variation1nstd206human GRCh38 chr4: 99,584,527-99,584,688 , GRCh37.p13 chr4: 100,505,684-100,505,845 MTTP
    nsv5346906translocation1nstd200human GRCh38 chr4: 99,601,387-99,601,387 , GRCh38 chr4: 99,601,471-99,601,471 , GRCh37.p13 chr4: 100,522,628-100,522,628 , GRCh37.p13 chr4: 100,522,544-100,522,544 MTTP
    nsv5332664translocation1nstd200human GRCh37 chr4: 100,484,597-100,484,597 , GRCh37 chr4: 100,483,981-100,483,981 , GRCh38.p12 chr4: 99,563,440-99,563,440 , GRCh38.p12 chr4: 99,562,824-99,562,824 MTTP, TRMT10A
    nsv5331488translocation1nstd200human GRCh37 chr4: 100,522,544-100,522,544 , GRCh37 chr4: 100,522,628-100,522,628 , GRCh38.p12 chr4: 99,601,387-99,601,387 , GRCh38.p12 chr4: 99,601,471-99,601,471 MTTP
    nsv5086517mobile element insertion1nstd203human GRCh38 chr4: 99,597,330-99,597,345 , GRCh37.p13 chr4: 100,518,487-100,518,502 MTTP
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