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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5909885copy number variation1nstd209human GRCh38 chr7: 20,170,675-20,171,226 , GRCh37.p13 chr7: 20,210,298-20,210,849 MACC1
    nsv5689503mobile element insertion2nstd211human GRCh38 chr7: 20,201,726-20,201,726 , GRCh37.p13 chr7: 20,241,349-20,241,349 MACC1
    nsv5685964mobile element insertion1nstd211human GRCh38 chr7: 20,212,817-20,212,817 , GRCh37.p13 chr7: 20,252,440-20,252,440 MACC1
    nsv5680489mobile element insertion1nstd211human GRCh38 chr7: 20,144,906-20,144,906 , GRCh37.p13 chr7: 20,184,529-20,184,529 MACC1-AS1, MACC1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5539660insertion1nstd206human GRCh38 chr7: 20,200,080-20,200,097 , GRCh37.p13 chr7: 20,239,703-20,239,720 MACC1
    nsv5473682copy number variation1nstd206human GRCh38 chr7: 20,193,335-20,193,389 , GRCh37.p13 chr7: 20,232,958-20,233,012 MACC1
    nsv5465026copy number variation1nstd206human GRCh38 chr7: 20,162,899-20,162,960 , GRCh37.p13 chr7: 20,202,522-20,202,583 MACC1
    nsv5461856copy number variation1nstd206human GRCh38 chr7: 20,180,986-20,182,101 , GRCh37.p13 chr7: 20,220,609-20,221,724 MACC1
    nsv5406328mobile element insertion1nstd206human GRCh38 chr7: 20,212,817-20,212,868 , GRCh37.p13 chr7: 20,252,440-20,252,491 MACC1
    nsv5404332mobile element insertion1nstd206human GRCh38 chr7: 20,201,726-20,201,777 , GRCh37.p13 chr7: 20,241,349-20,241,400 MACC1
    nsv5370384translocation1nstd200human GRCh38 chr7: 20,208,235-20,208,235 , GRCh38 chr7: 20,208,317-20,208,317 , GRCh37.p13 chr7: 20,247,858-20,247,858 , GRCh37.p13 chr7: 20,247,940-20,247,940 MACC1
    nsv5353860translocation1nstd200human GRCh38 chr21: 44,806,231-44,806,231 , GRCh38 chr7: 20,216,910-20,216,910 , GRCh37.p13 chr21: 46,226,146-46,226,146 , GRCh37.p13 chr7: 20,256,533-20,256,533 SUMO3, MACC1, 1 more genes
    nsv5235443copy number variation1nstd204human GRCh38.p13 chr7: 20,160,901-20,163,700 , GRCh37.p13 chr7: 20,200,524-20,203,323 MACC1
    nsv5180644mobile element insertion1nstd203human GRCh38 chr7: 20,151,238-20,151,256 , GRCh37.p13 chr7: 20,190,861-20,190,879 MACC1, MACC1-AS1
    nsv5174922mobile element insertion1nstd203human GRCh38 chr7: 20,185,478-20,185,481 , GRCh37.p13 chr7: 20,225,101-20,225,104 MACC1
    nsv5119239mobile element insertion1nstd203human GRCh38 chr7: 20,201,708-20,201,726 , GRCh37.p13 chr7: 20,241,331-20,241,349 MACC1
    nsv5116749mobile element insertion1nstd203human GRCh38 chr7: 20,201,714-20,201,726 , GRCh37.p13 chr7: 20,241,337-20,241,349 MACC1
    nsv5112974mobile element insertion1nstd203human GRCh38 chr7: 20,201,715-20,201,726 , GRCh37.p13 chr7: 20,241,338-20,241,349 MACC1
    nsv5109198mobile element insertion1nstd203human GRCh38 chr7: 20,201,712-20,201,723 , GRCh37.p13 chr7: 20,241,335-20,241,346 MACC1
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