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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973271inversion1nstd209human GRCh38 chr10: 79,614,541-79,672,309 , GRCh37.p13 chr10: 81,374,297-81,432,065 SFTPA1, LOC101929506, 1 more genes
    nsv5958078insertion1nstd209human GRCh38 chr10: 79,641,418-79,641,418 , GRCh37.p13 chr10: 81,401,174-81,401,174 LINC02679
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5909430copy number variation1nstd209human GRCh38 chr10: 79,617,422-79,627,798 , GRCh37.p13 chr10: 81,377,178-81,387,554 LINC02679
    nsv5866455copy number variation1nstd209human GRCh38 chr10: 79,656,837-79,658,718 , GRCh37.p13 chr10: 81,416,593-81,418,474 LINC02679
    nsv5866100copy number variation1nstd209human GRCh38 chr10: 79,617,395-79,627,294 , GRCh37.p13 chr10: 81,377,151-81,387,050 LINC02679
    nsv5724079mobile element insertion2nstd211human GRCh38 chr10: 79,631,427-79,631,427 , GRCh37.p13 chr10: 81,391,183-81,391,183 LINC02679
    nsv5710572mobile element insertion1nstd211human GRCh38 chr10: 79,647,609-79,647,609 , GRCh37.p13 chr10: 81,407,365-81,407,365 LINC02679
    nsv5702810mobile element insertion1nstd211human GRCh38 chr10: 79,647,610-79,647,610 , GRCh37.p13 chr10: 81,407,366-81,407,366 LINC02679
    nsv5672415inversion1nstd207human GRCh38 chr10: 79,542,902-80,213,948 , GRCh37.p13 chr10: 81,302,658-81,973,704 , ANXA11, 30 more genes
    nsv5643766insertion1nstd207human GRCh38 chr10: 79,641,912-79,641,912 , GRCh37.p13 chr10: 81,401,668-81,401,668 LINC02679
    nsv5641482insertion1nstd207human GRCh38 chr10: 79,639,924-79,639,924 , GRCh37.p13 chr10: 81,399,680-81,399,680 LINC02679
    nsv5638576insertion1nstd207human GRCh38 chr10: 79,660,490-79,660,490 , GRCh37.p13 chr10: 81,420,246-81,420,246 LINC02679
    nsv5635184insertion1nstd207human GRCh38 chr10: 79,641,883-79,641,883 , GRCh37.p13 chr10: 81,401,639-81,401,639 LINC02679
    nsv5634941insertion2nstd207human GRCh38 chr10: 79,641,418-79,641,418 , GRCh37.p13 chr10: 81,401,174-81,401,174 LINC02679
    nsv5633443insertion1nstd207human GRCh38 chr10: 79,650,172-79,650,172 , GRCh37.p13 chr10: 81,409,928-81,409,928 LINC02679
    nsv5599338copy number variation1nstd207human GRCh38 chr10: 79,649,810-79,650,172 , GRCh37.p13 chr10: 81,409,566-81,409,928 LINC02679
    nsv5596873copy number variation1nstd207human GRCh38 chr10: 79,633,715-79,634,073 , GRCh37.p13 chr10: 81,393,471-81,393,829 LINC02679
    nsv5593163copy number variation1nstd207human GRCh38 chr10: 79,644,512-79,645,007 , GRCh37.p13 chr10: 81,404,268-81,404,763 LINC02679
    nsv5590795copy number variation1nstd207human GRCh38 chr10: 79,632,066-79,632,371 , GRCh37.p13 chr10: 81,391,822-81,392,127 LINC02679
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