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Items: 1 to 20 of 486

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964192insertion1nstd209human GRCh38 chr1: 92,305,432-92,305,432 , GRCh37.p13 chr1: 92,770,989-92,770,989 GLMN, RPAP2
    nsv5882353copy number variation1nstd209human GRCh38 chr1: 92,347,778-92,347,917 , GRCh37.p13 chr1: 92,813,335-92,813,474 GLMN, RPAP2
    nsv5871981copy number variation1nstd209human GRCh38 chr1: 92,379,698-92,380,040 , GRCh37.p13 chr1: 92,845,255-92,845,597 GLMN, RPAP2
    nsv5871598copy number variation1nstd209human GRCh38 chr1: 92,384,930-92,385,088 , GRCh37.p13 chr1: 92,850,487-92,850,645 GLMN, RPAP2
    nsv5871072copy number variation1nstd209human GRCh38 chr1: 92,309,536-92,309,595 , GRCh37.p13 chr1: 92,775,093-92,775,152 GLMN, RPAP2
    nsv5680623mobile element insertion1nstd211human GRCh38 chr1: 92,271,430-92,271,430 , GRCh37.p13 chr1: 92,736,987-92,736,987 GLMN
    nsv5678849mobile element insertion1nstd211human GRCh38 chr1: 92,392,996-92,392,996 , GRCh37.p13 chr1: 92,858,553-92,858,553 GLMN, RPAP2
    nsv5568114copy number variation1nstd207human GRCh38 chr1: 92,309,536-92,309,595 , GRCh37.p13 chr1: 92,775,093-92,775,152 RPAP2, GLMN
    nsv5429353copy number variation1nstd206human GRCh38 chr1: 92,384,944-92,385,089 , GRCh37.p13 chr1: 92,850,501-92,850,646 GLMN, RPAP2
    nsv5428967copy number variation1nstd206human GRCh38 chr1: 92,273,949-92,274,212 , GRCh37.p13 chr1: 92,739,506-92,739,769 GLMN
    nsv5421790copy number variation1nstd206human GRCh38 chr1: 92,356,308-92,356,361 , GRCh37.p13 chr1: 92,821,865-92,821,918 RPAP2, GLMN
    nsv5420703copy number variation1nstd206human GRCh38 chr1: 92,347,781-92,347,918 , GRCh37.p13 chr1: 92,813,338-92,813,475 GLMN, RPAP2
    nsv5420091copy number variation1nstd206human GRCh38 chr1: 92,431,821-92,433,019 , GRCh37.p13 chr1: 92,897,378-92,898,576 GLMN
    nsv5416400copy number variation1nstd206human GRCh38 chr1: 92,335,754-92,335,919 , GRCh37.p13 chr1: 92,801,311-92,801,476 GLMN, RPAP2
    nsv5415510copy number variation1nstd206human GRCh38 chr1: 92,427,409-92,435,807 , GRCh37.p13 chr1: 92,892,966-92,901,364 GLMN
    nsv5414736copy number variation1nstd206human GRCh38 chr1: 92,435,264-92,435,368 , GRCh37.p13 chr1: 92,900,821-92,900,925 GLMN
    nsv5406784mobile element insertion1nstd206human GRCh38 chr1: 92,271,430-92,271,481 , GRCh37.p13 chr1: 92,736,987-92,737,038 GLMN
    nsv5405186mobile element insertion1nstd206human GRCh38 chr1: 92,392,996-92,393,047 , GRCh37.p13 chr1: 92,858,553-92,858,604 RPAP2, GLMN
    nsv5353580translocation1nstd200human GRCh38 chr1: 92,427,957-92,427,957 , GRCh38 chr1: 92,427,881-92,427,881 , GRCh37.p13 chr1: 92,893,514-92,893,514 , GRCh37.p13 chr1: 92,893,438-92,893,438 GLMN
    nsv5336687translocation1nstd200human GRCh37 chr1: 92,893,438-92,893,438 , GRCh37 chr1: 92,893,514-92,893,514 , GRCh38.p12 chr1: 92,427,881-92,427,881 , GRCh38.p12 chr1: 92,427,957-92,427,957 GLMN
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