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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6119067copy number variation1nstd186human GRCh37 chr4: 83,824,549-83,825,448 , GRCh38.p12 chr4: 82,903,396-82,904,295 THAP9
    nsv5891510copy number variation1nstd209human GRCh38 chr4: 82,903,411-82,904,253 , GRCh37.p13 chr4: 83,824,564-83,825,406 THAP9
    nsv5690699mobile element insertion1nstd211human GRCh38 chr4: 82,901,653-82,901,653 , GRCh37.p13 chr4: 83,822,806-83,822,806 THAP9
    nsv5682023mobile element insertion2nstd211human GRCh38 chr4: 82,914,838-82,914,838 , GRCh37.p13 chr4: 83,835,991-83,835,991 THAP9
    nsv5676503mobile element insertion2nstd211human GRCh38 chr4: 82,919,335-82,919,335 , GRCh37.p13 chr4: 83,840,488-83,840,488 THAP9
    nsv5619341insertion1nstd207human GRCh38 chr4: 82,904,059-82,904,059 , GRCh37.p13 chr4: 83,825,212-83,825,212 THAP9
    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
    nsv5469327copy number variation1nstd206human GRCh38 chr4: 82,914,732-82,914,792 , GRCh37.p13 chr4: 83,835,885-83,835,945 THAP9
    nsv5467606copy number variation1nstd206human GRCh38 chr4: 82,903,396-82,904,295 , GRCh37.p13 chr4: 83,824,549-83,825,448 THAP9
    nsv5405477mobile element insertion1nstd206human GRCh38 chr4: 82,914,838-82,914,889 , GRCh37.p13 chr4: 83,835,991-83,836,042 THAP9
    nsv5404195mobile element insertion1nstd206human GRCh38 chr4: 82,901,653-82,901,704 , GRCh37.p13 chr4: 83,822,806-83,822,857 THAP9
    nsv5400667mobile element insertion1nstd206human GRCh38 chr4: 82,919,335-82,919,386 , GRCh37.p13 chr4: 83,840,488-83,840,539 THAP9
    nsv5387212copy number variation1nstd186human GRCh37 chr4: 83,824,532-83,825,488 , GRCh38.p12 chr4: 82,903,379-82,904,335 THAP9
    nsv5307811copy number variation1nstd204human GRCh38.p13 chr4: 82,902,944-82,904,595 , GRCh37.p13 chr4: 83,824,097-83,825,748 THAP9
    nsv5086819mobile element insertion1nstd203human GRCh38 chr4: 82,914,824-82,914,838 , GRCh37.p13 chr4: 83,835,977-83,835,991 THAP9
    nsv5040446inversion1nstd200human GRCh38 chr4: 76,223,829-89,968,114 , GRCh37.p13 chr4: 77,144,982-90,889,265 , KPNA2P1, 209 more genes
    nsv5037291inversion1nstd200human GRCh38 chr4: 74,160,096-84,998,626 , GRCh37.p13 chr4: 75,025,813-85,919,779 , LOC105377302, 175 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
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