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Items: 1 to 20 of 767

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048435inversion1nstd229human GRCh38 chr2: 33,516,869-33,522,119 , GRCh37.p13 chr2: 33,741,936-33,747,186 RASGRP3
    nsv7047639inversion1nstd229human GRCh38 chr2: 29,857,017-35,800,286 , GRCh37.p13 chr2: 30,079,883-36,025,352 LTBP1, KRT18P52, 67 more genes
    nsv6677640copy number variation1nstd229human GRCh38 chr2: 33,468,670-33,471,453 , GRCh37.p13 chr2: 33,693,737-33,696,520 RASGRP3
    nsv6676368copy number variation1nstd229human GRCh38 chr2: 33,443,119-33,460,259 , GRCh37.p13 chr2: 33,668,186-33,685,326 RASGRP3
    nsv6676363copy number variation1nstd229human GRCh38 chr2: 33,564,901-33,582,100 , GRCh37.p13 chr2: 33,789,968-33,807,167 RASGRP3-AS1, RASGRP3, 1 more genes
    nsv6676225copy number variation1nstd229human GRCh38 chr2: 33,492,026-33,496,997 , GRCh37.p13 chr2: 33,717,093-33,722,064 RASGRP3
    nsv6676178copy number variation1nstd229human GRCh38 chr2: 33,506,071-33,509,403 , GRCh37.p13 chr2: 33,731,138-33,734,470 RASGRP3
    nsv6674889copy number variation1nstd229human GRCh38 chr2: 33,499,418-33,499,607 , GRCh37.p13 chr2: 33,724,485-33,724,674 RASGRP3
    nsv6672295copy number variation1nstd229human GRCh38 chr2: 33,492,045-33,502,802 , GRCh37.p13 chr2: 33,717,112-33,727,869 RASGRP3
    nsv6672256copy number variation1nstd229human GRCh38 chr2: 33,441,586-33,474,257 , GRCh37.p13 chr2: 33,666,653-33,699,324 RASGRP3
    nsv6671747copy number variation1nstd229human GRCh38 chr2: 33,556,218-33,556,546 , GRCh37.p13 chr2: 33,781,285-33,781,613 RASGRP3-AS1, RASGRP3
    nsv6671451copy number variation1nstd229human GRCh38 chr2: 33,518,819-33,527,440 , GRCh37.p13 chr2: 33,743,886-33,752,507 RASGRP3
    nsv6671120copy number variation1nstd229human GRCh38 chr2: 33,485,240-33,491,307 , GRCh37.p13 chr2: 33,710,307-33,716,374 RASGRP3
    nsv6670966copy number variation1nstd229human GRCh38 chr2: 33,531,909-33,531,966 , GRCh37.p13 chr2: 33,756,976-33,757,033 RASGRP3
    nsv6670622copy number variation1nstd229human GRCh38 chr2: 33,446,453-33,501,504 , GRCh37.p13 chr2: 33,671,520-33,726,571 RASGRP3
    nsv6670453copy number variation1nstd229human GRCh38 chr2: 33,464,695-33,468,926 , GRCh37.p13 chr2: 33,689,762-33,693,993 RASGRP3
    nsv6669660copy number variation1nstd229human GRCh38 chr2: 33,471,784-33,480,462 , GRCh37.p13 chr2: 33,696,851-33,705,529 RASGRP3
    nsv6669165copy number variation1nstd229human GRCh38 chr2: 33,494,001-33,494,304 , GRCh37.p13 chr2: 33,719,068-33,719,371 RASGRP3
    nsv6668203copy number variation1nstd229human GRCh38 chr2: 33,416,801-33,435,800 , GRCh37.p13 chr2: 33,641,868-33,660,867 RASGRP3, MIR4430
    nsv6667304copy number variation1nstd229human GRCh38 chr2: 33,463,586-33,470,813 , GRCh37.p13 chr2: 33,688,653-33,695,880 RASGRP3
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