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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959735insertion1nstd209human GRCh38 chr5: 17,171,601-17,171,601 , GRCh37.p13 chr5: 17,171,710-17,171,710 BASP1-AS1, LOC105374664
    nsv5957682insertion1nstd209human GRCh38 chr5: 17,205,640-17,205,640 , GRCh37.p13 chr5: 17,205,749-17,205,749 BASP1-AS1
    nsv5957485insertion1nstd209human GRCh38 chr5: 17,172,042-17,172,042 , GRCh37.p13 chr5: 17,172,151-17,172,151 BASP1-AS1, LOC105374664
    nsv5953948insertion1nstd209human GRCh38 chr5: 17,130,361-17,130,361 , GRCh37.p13 chr5: 17,130,470-17,130,470 BASP1-AS1
    nsv5950194insertion1nstd209human GRCh38 chr5: 17,212,992-17,212,992 , GRCh37.p13 chr5: 17,213,101-17,213,101 BASP1-AS1
    nsv5903069copy number variation1nstd209human GRCh38 chr5: 17,136,267-17,140,249 , GRCh37.p13 chr5: 17,136,376-17,140,358 BASP1-AS1
    nsv5898199copy number variation1nstd209human GRCh38 chr5: 17,140,532-17,141,143 , GRCh37.p13 chr5: 17,140,641-17,141,252 BASP1-AS1
    nsv5891288copy number variation1nstd209human GRCh38 chr5: 17,207,326-17,208,491 , GRCh37.p13 chr5: 17,207,435-17,208,600 BASP1-AS1
    nsv5890084copy number variation1nstd209human GRCh38 chr5: 17,146,617-17,146,668 , GRCh37.p13 chr5: 17,146,726-17,146,777 BASP1-AS1
    nsv5842188copy number variation1nstd209human GRCh38 chr5: 17,136,190-17,140,089 , GRCh37.p13 chr5: 17,136,299-17,140,198 BASP1-AS1
    nsv5684110mobile element insertion2nstd211human GRCh38 chr5: 17,130,376-17,130,376 , GRCh37.p13 chr5: 17,130,485-17,130,485 BASP1-AS1
    nsv5680513mobile element insertion1nstd211human GRCh38 chr5: 17,205,658-17,205,658 , GRCh37.p13 chr5: 17,205,767-17,205,767 BASP1-AS1
    nsv5634163insertion1nstd207human GRCh38 chr5: 17,172,042-17,172,042 , GRCh37.p13 chr5: 17,172,151-17,172,151 LOC105374664, BASP1-AS1
    nsv5543765insertion1nstd206human GRCh38 chr5: 17,172,042-17,172,042 , GRCh37.p13 chr5: 17,172,151-17,172,151 BASP1-AS1, LOC105374664
    nsv5398932mobile element insertion1nstd206human GRCh38 chr5: 17,205,658-17,205,709 , GRCh37.p13 chr5: 17,205,767-17,205,818 BASP1-AS1
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv5333519translocation1nstd200human GRCh37 chr5: 17,140,641-17,140,641 , GRCh37 chr5: 17,140,066-17,140,066 , GRCh38.p12 chr5: 17,139,957-17,139,957 , GRCh38.p12 chr5: 17,140,532-17,140,532 BASP1-AS1
    nsv5095823mobile element insertion1nstd203human GRCh38 chr5: 17,130,360-17,130,376 , GRCh37.p13 chr5: 17,130,469-17,130,485 BASP1-AS1
    nsv5090971mobile element insertion1nstd203human GRCh38 chr5: 17,130,376-17,130,381 , GRCh37.p13 chr5: 17,130,485-17,130,490 BASP1-AS1
    nsv5088219mobile element insertion1nstd203human GRCh38 chr5: 17,130,361-17,130,376 , GRCh37.p13 chr5: 17,130,470-17,130,485 BASP1-AS1
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