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Items: 1 to 20 of 302

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5897704copy number variation1nstd209human GRCh37.p13 chr5: 51,758,667-52,335,868 , GRCh38 chr5: 52,462,833-53,040,038 , ITGA1, 6 more genes
    nsv5725597mobile element insertion1nstd211human GRCh38 chr5: 53,035,857-53,035,857 , GRCh37.p13 chr5: 52,331,687-52,331,687 ITGA2
    nsv5464685copy number variation1nstd206human GRCh38 chr5: 53,089,033-53,089,297 , GRCh37.p13 chr5: 52,384,863-52,385,127 ITGA2
    nsv5368371translocation1nstd200human GRCh38 chr5: 53,089,297-53,089,297 , GRCh38 chr5: 53,089,033-53,089,033 , GRCh37.p13 chr5: 52,384,863-52,384,863 , GRCh37.p13 chr5: 52,385,127-52,385,127 ITGA2
    nsv5368370translocation1nstd200human GRCh38 chr5: 53,064,667-53,064,667 , GRCh38 chr10: 85,725,041-85,725,041 , GRCh37.p13 chr10: 87,484,798-87,484,798 , GRCh37.p13 chr5: 52,360,497-52,360,497 ITGA2, GRID1
    nsv5368369translocation1nstd200human GRCh38 chr5: 53,064,659-53,064,659 , GRCh38 chr10: 85,724,213-85,724,213 , GRCh37.p13 chr10: 87,483,970-87,483,970 , GRCh37.p13 chr5: 52,360,489-52,360,489 ITGA2, GRID1
    nsv5084579mobile element insertion1nstd203human GRCh38 chr5: 53,032,160-53,032,174 , GRCh37.p13 chr5: 52,327,990-52,328,004 ITGA2
    nsv4931515copy number variation1nstd200human GRCh38 chr5: 53,040,756-53,041,990 , GRCh37.p13 chr5: 52,336,586-52,337,820 ITGA2
    nsv4802988copy number variation1nstd200human GRCh37 chr5: 52,384,863-52,385,127 , GRCh38.p12 chr5: 53,089,033-53,089,297 ITGA2
    nsv4728831copy number variation1nstd102humanPathogenic GRCh37 chr5: 49,430,268-53,182,665 , GRCh38.p12 chr5: 50,134,434-53,886,835 LOC107986380, RPS17P11, 34 more genes
    nsv4680481copy number variation1nstd189human GRCh37.p13 chr5: 52,227,239-52,641,986 , GRCh38.p12 chr5: 52,931,409-53,346,156 ITGA1, ITGA2, 5 more genes
    nsv4593154copy number variation1nstd183human GRCh37 chr5: 52,377,181-52,436,868 , GRCh38.p12 chr5: 53,081,351-53,141,038 MOCS2, ITGA2, 1 more genes
    nsv4571656mobile element insertion1nstd166human GRCh37.p13 chr5: 52,331,671-52,331,671 , GRCh38.p12 chr5: 53,035,841-53,035,841 ITGA2
    nsv4565737mobile element insertion1nstd166human GRCh37.p13 chr5: 52,288,551-52,288,551 , GRCh38.p12 chr5: 52,992,721-52,992,721 ITGA2
    nsv4522172copy number variation1nstd166human GRCh37.p13 chr5: 52,384,863-52,385,127 , GRCh38.p12 chr5: 53,089,033-53,089,297 ITGA2
    nsv4478225mobile element insertion1nstd166human GRCh37.p13 chr5: 52,333,096-52,333,096 , GRCh38.p12 chr5: 53,037,266-53,037,266 ITGA2
    nsv4478224mobile element insertion1nstd166human GRCh37.p13 chr5: 52,292,601-52,292,601 , GRCh38.p12 chr5: 52,996,771-52,996,771 ITGA2
    nsv4477900mobile element insertion1nstd166human GRCh37.p13 chr5: 52,297,690-52,297,690 , GRCh38.p12 chr5: 53,001,860-53,001,860 ITGA2
    nsv4477766mobile element insertion1nstd166human GRCh37.p13 chr5: 52,355,636-52,355,636 , GRCh38.p12 chr5: 53,059,806-53,059,806 ITGA2
    nsv4456673copy number variation1nstd102humanUncertain significance GRCh37 chr5: 52,053,923-52,680,028 , GRCh38.p12 chr5: 52,758,089-53,384,198 ITGA2, MOCS2-DT, 8 more genes
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