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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6111103inversion1nstd212human GRCh38 chr5: 99,513,922-100,390,410 , GRCh37.p13 chr5: 98,849,626-99,726,114 , CRLF3P2, 17 more genes
    nsv6107040inversion1nstd212human GRCh37.p13 chr5: 99,723,514-99,899,435 , GRCh38 chr5: 100,387,810-100,563,731 , FAM174A, 2 more genes
    nsv6061393insertion1nstd212human GRCh38 chr5: 100,390,711-100,390,711 , GRCh37.p13 chr5: 99,726,415-99,726,415
    nsv6060486insertion1nstd212human GRCh38 chr5: 100,389,895-100,389,895 , GRCh37.p13 chr5: 99,725,599-99,725,599
    nsv6017590copy number variation1nstd212human GRCh38 chr5: 100,390,257-100,392,717 , GRCh37.p13 chr5: 99,725,961-99,728,421
    nsv6015242copy number variation1nstd212human GRCh38 chr5: 100,389,765-100,389,891 , GRCh37.p13 chr5: 99,725,469-99,725,595
    nsv6002206copy number variation1nstd212human GRCh38 chr5: 100,389,895-100,390,714 , GRCh37.p13 chr5: 99,725,599-99,726,418
    nsv5840570copy number variation2nstd209human GRCh38 chr5: 100,387,798-100,395,078 , GRCh37.p13 chr5: 99,723,502-99,730,782 , GUSBP19, 1 more genes
    nsv5840242copy number variation1nstd209human GRCh38 chr5: 100,384,488-100,388,132 , GRCh37.p13 chr5: 99,720,192-99,723,836 , GUSBP19
    nsv5839933copy number variation2nstd209human GRCh38 chr5: 100,384,700-100,391,813 , GRCh37.p13 chr5: 99,720,404-99,727,517 , GUSBP19
    nsv5637196insertion1nstd207human GRCh38 chr5: 100,390,465-100,390,465 , GRCh37.p13 chr5: 99,726,169-99,726,169
    nsv5631227insertion1nstd207human GRCh38 chr5: 100,390,488-100,390,488 , GRCh37.p13 chr5: 99,726,192-99,726,192
    nsv5628573insertion1nstd207human GRCh38 chr5: 100,391,752-100,391,752 , GRCh37.p13 chr5: 99,727,456-99,727,456
    nsv5578360copy number variation1nstd207human GRCh38 chr5: 100,390,001-100,390,819 , GRCh37.p13 chr5: 99,725,705-99,726,523
    nsv5565650copy number variation1nstd207human GRCh38 chr5: 100,389,159-100,389,329 , GRCh37.p13 chr5: 99,724,863-99,725,033
    nsv5418271copy number variation1nstd206human GRCh38 chr5: 100,390,117-100,392,550 , GRCh37.p13 chr5: 99,725,821-99,728,254
    nsv5315492copy number variation1nstd204human GRCh37.p13 chr5: 99,694,650-99,993,103 , GRCh38.p13 chr5: 100,358,946-100,657,399 , FAM174A, 2 more genes
    nsv5237467copy number variation1nstd204human GRCh38.p13 chr5: 100,390,656-100,391,813 , GRCh37.p13 chr5: 99,726,360-99,727,517
    nsv5227126copy number variation1nstd204human GRCh38.p13 chr5: 100,385,304-100,387,643 , GRCh37.p13 chr5: 99,721,008-99,723,347 , GUSBP19
    nsv5224863copy number variation1nstd204human GRCh38.p13 chr5: 100,385,504-100,391,003 , GRCh37.p13 chr5: 99,721,208-99,726,707 , GUSBP19
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