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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056095inversion1nstd229human GRCh38 chr5: 52,719,057-53,664,749 , GRCh37.p13 chr5: 52,014,891-52,960,579 B3GNTL1P1, RPL17P21, 11 more genes
    nsv7049418inversion1nstd229human GRCh38 chr5: 52,184,974-52,821,825 , GRCh37.p13 chr5: 51,480,808-52,117,659 MFSD4BP1, RPS17P11, 3 more genes
    nsv7047220inversion1nstd229human GRCh38 chr5: 52,892,408-52,897,995 , GRCh37.p13 chr5: 52,188,239-52,193,825 ITGA1
    nsv7041849inversion1nstd229human GRCh38 chr5: 52,908,208-52,908,242 , GRCh37.p13 chr5: 52,204,038-52,204,072 ITGA1
    nsv6774778copy number variation1nstd229human GRCh38 chr5: 52,761,698-52,830,465 , GRCh37.p13 chr5: 52,057,532-52,126,299 PELO, ITGA1
    nsv6774307copy number variation1nstd229human GRCh38 chr5: 52,674,289-52,805,131 , GRCh37.p13 chr5: 51,970,123-52,100,965 ITGA1, PELO
    nsv6773571copy number variation1nstd229human GRCh38 chr5: 52,896,357-52,896,549 , GRCh37.p13 chr5: 52,192,188-52,192,380 ITGA1
    nsv6773001copy number variation1nstd229human GRCh38 chr5: 52,817,231-52,820,147 , GRCh37.p13 chr5: 52,113,065-52,115,981 ITGA1
    nsv6772767copy number variation1nstd229human GRCh38 chr5: 52,889,088-52,889,116 , GRCh37.p13 chr5: 52,184,920-52,184,948 B3GNTL1P1, ITGA1
    nsv6771185copy number variation1nstd229human GRCh38 chr5: 52,884,679-52,884,887 , GRCh37.p13 chr5: 52,180,511-52,180,719 ITGA1
    nsv6771178copy number variation1nstd229human GRCh38 chr5: 52,824,391-52,840,186 , GRCh37.p13 chr5: 52,120,225-52,136,020 ITGA1
    nsv6766352copy number variation1nstd229human GRCh38 chr5: 52,086,933-59,394,572 , GRCh37.p13 chr5: 51,382,767-58,690,398 , LOC105378980, 102 more genes
    nsv6765965copy number variation1nstd229human GRCh38 chr5: 52,913,101-52,938,800 , GRCh37.p13 chr5: 52,208,931-52,234,630 ITGA1
    nsv6765959copy number variation1nstd229human GRCh38 chr5: 52,859,701-52,862,400 , GRCh37.p13 chr5: 52,155,535-52,158,234 ITGA1
    nsv6764979copy number variation1nstd229human GRCh38 chr5: 52,789,923-52,790,043 , GRCh37.p13 chr5: 52,085,757-52,085,877 PELO, ITGA1
    nsv6764629copy number variation1nstd229human GRCh38 chr5: 52,868,401-52,874,900 , GRCh37.p13 chr5: 52,164,235-52,170,734 ITGA1
    nsv6763381copy number variation1nstd229human GRCh38 chr5: 52,823,386-52,824,541 , GRCh37.p13 chr5: 52,119,220-52,120,375 ITGA1
    nsv6761890copy number variation1nstd229human GRCh38 chr5: 52,884,106-52,887,479 , GRCh37.p13 chr5: 52,179,938-52,183,311 ITGA1
    nsv6761229copy number variation1nstd229human GRCh38 chr5: 52,935,958-52,936,274 , GRCh37.p13 chr5: 52,231,788-52,232,104 ITGA1
    nsv6760780copy number variation1nstd229human GRCh38 chr5: 52,952,327-52,957,816 , GRCh37.p13 chr5: 52,248,157-52,253,646 ITGA1
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