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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959226insertion1nstd209human GRCh38 chr9: 120,834,376-120,834,376 , GRCh37.p13 chr9: 123,596,654-123,596,654 PSMD5
    nsv5927443copy number variation1nstd209human GRCh38 chr9: 120,822,935-120,823,051 , GRCh37.p13 chr9: 123,585,213-123,585,329 PSMD5
    nsv5924696copy number variation1nstd209human GRCh38 chr9: 120,840,537-120,840,710 , GRCh37.p13 chr9: 123,602,815-123,602,988 PSMD5
    nsv5848055copy number variation1nstd209human GRCh38 chr9: 120,818,277-120,819,276 , GRCh37.p13 chr9: 123,580,555-123,581,554 PSMD5
    nsv5699260mobile element insertion1nstd211human GRCh38 chr9: 120,834,393-120,834,393 , GRCh37.p13 chr9: 123,596,671-123,596,671 PSMD5
    nsv5474966copy number variation1nstd206human GRCh38 chr9: 120,824,436-120,824,516 , GRCh37.p13 chr9: 123,586,714-123,586,794 PSMD5
    nsv5407787mobile element insertion1nstd206human GRCh38 chr9: 120,834,393-120,834,444 , GRCh37.p13 chr9: 123,596,671-123,596,722 PSMD5
    nsv5373062translocation1nstd200human GRCh38 chr9: 120,816,184-120,816,184 , GRCh38 chr9: 120,816,266-120,816,266 , GRCh37.p13 chr9: 123,578,462-123,578,462 , GRCh37.p13 chr9: 123,578,544-123,578,544 PSMD5
    nsv5139954mobile element insertion1nstd203human GRCh38 chr9: 120,823,910-120,823,924 , GRCh37.p13 chr9: 123,586,188-123,586,202 PSMD5
    nsv5121233mobile element insertion1nstd203human GRCh38 chr9: 120,834,376-120,834,393 , GRCh37.p13 chr9: 123,596,654-123,596,671 PSMD5
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983497copy number variation1nstd200human GRCh38 chr9: 120,833,667-120,833,803 , GRCh37.p13 chr9: 123,595,945-123,596,081 PSMD5
    nsv4830416copy number variation1nstd200human GRCh37 chr9: 123,596,208-123,617,768 , GRCh38.p12 chr9: 120,833,930-120,855,490 PHF19, PSMD5, 1 more genes
    nsv4542006insertion1nstd166human GRCh37.p13 chr9: 123,596,654-123,596,654 , GRCh38.p12 chr9: 120,834,376-120,834,376 PSMD5
    nsv4482421mobile element insertion1nstd166human GRCh37.p13 chr9: 123,586,188-123,586,188 , GRCh38.p12 chr9: 120,823,910-120,823,910 PSMD5
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4435613copy number variation1nstd172human GRCh37.p13 chr9: 123,569,001-123,577,000 , GRCh38.p12 chr9: 120,806,723-120,814,722 PSMD5
    nsv4343265sequence alteration1nstd166human GRCh37.p13 chr9: 123,579,171-124,453,597 , GRCh38.p12 chr9: 120,816,893-121,691,318 C5, GSN, 17 more genes
    nsv4337792sequence alteration1nstd166human GRCh37.p13 chr9: 123,581,947-123,585,653 , GRCh38.p12 chr9: 120,819,669-120,823,375 PSMD5
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