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Items: 1 to 20 of 304

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142885insertion1nstd232human GRCh37.p13 chr5: 43,702,840-43,702,840 , GRCh38.p12 chr5: 43,702,738-43,702,738 NNT
    nsv7056675inversion1nstd229human GRCh38 chr5: 43,705,116-43,710,275 , GRCh37.p13 chr5: 43,705,218-43,710,377 NNT
    nsv6776939copy number variation1nstd229human GRCh38 chr5: 43,648,494-43,652,762 , GRCh37.p13 chr5: 43,648,596-43,652,864 NNT
    nsv6776434copy number variation1nstd229human GRCh38 chr5: 43,662,801-43,671,100 , GRCh37.p13 chr5: 43,662,903-43,671,202 RPL29P12, NNT
    nsv6774499copy number variation1nstd229human GRCh38 chr5: 43,679,654-43,694,791 , GRCh37.p13 chr5: 43,679,756-43,694,893 NNT
    nsv6773285copy number variation1nstd229human GRCh38 chr5: 43,626,072-43,626,166 , GRCh37.p13 chr5: 43,626,174-43,626,268 NNT
    nsv6769628copy number variation1nstd229human GRCh38 chr5: 43,685,801-43,691,700 , GRCh37.p13 chr5: 43,685,903-43,691,802 NNT
    nsv6767464copy number variation1nstd229human GRCh38 chr5: 43,596,577-43,600,320 , GRCh37.p13 chr5: 43,596,679-43,600,422 NNT-AS1, NNT
    nsv6767368copy number variation1nstd229human GRCh38 chr5: 43,281,116-43,944,609 , GRCh37.p13 chr5: 43,281,218-43,944,711 TMEM267, C5orf34-AS1, 11 more genes
    nsv6763866copy number variation1nstd229human GRCh38 chr5: 43,598,737-44,098,400 , GRCh37.p13 chr5: 43,598,839-44,098,502 RPL29P12, NNT, 2 more genes
    nsv6762657copy number variation1nstd229human GRCh38 chr5: 43,684,991-43,685,513 , GRCh37.p13 chr5: 43,685,093-43,685,615 NNT
    nsv6762022copy number variation1nstd229human GRCh38 chr5: 43,618,094-43,618,241 , GRCh37.p13 chr5: 43,618,196-43,618,343 NNT
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6557495inversion1nstd223human GRCh38 chr5: 43,680,999-43,681,680 , GRCh37.p13 chr5: 43,681,101-43,681,782 NNT
    nsv6394770copy number variation1nstd223human GRCh38 chr5: 43,704,942-43,705,414 , GRCh37.p13 chr5: 43,705,044-43,705,516 NNT
    nsv6391404copy number variation1nstd223human GRCh38 chr5: 43,684,632-43,685,131 , GRCh37.p13 chr5: 43,684,734-43,685,233 NNT
    nsv6390305copy number variation1nstd223human GRCh38 chr5: 43,639,101-43,640,900 , GRCh37.p13 chr5: 43,639,203-43,641,002 NNT
    nsv6389056copy number variation1nstd223human GRCh38 chr5: 43,626,070-43,626,166 , GRCh37.p13 chr5: 43,626,172-43,626,268 NNT
    nsv6388398copy number variation1nstd223human GRCh38 chr5: 43,639,433-43,640,074 , GRCh37.p13 chr5: 43,639,535-43,640,176 NNT
    nsv6386815copy number variation1nstd223human GRCh38 chr5: 43,632,201-43,632,900 , GRCh37.p13 chr5: 43,632,303-43,633,002 NNT
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