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Items: 1 to 20 of 244

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5705517mobile element insertion1nstd211human GRCh38 chr22: 29,787,341-29,787,341 , GRCh37.p13 chr22: 30,183,330-30,183,330 ASCC2
    nsv5697099mobile element insertion2nstd211human GRCh38 chr22: 29,833,299-29,833,299 , GRCh37.p13 chr22: 30,229,288-30,229,288 ASCC2
    nsv5673427copy number variation1nstd102humanPathogenic GRCh37 chr22: 29,083,885-30,337,586 , GRCh38.p12 chr22: 28,687,897-29,941,597 SNORD125, RASL10A, 36 more genes
    nsv5673351copy number variation1nstd102humanPathogenic GRCh37 chr22: 29,105,984-30,337,586 , GRCh38.p12 chr22: 28,709,996-29,941,597 SNORD125, RASL10A, 36 more genes
    nsv5596982copy number variation1nstd207human GRCh38 chr22: 29,818,403-29,818,458 , GRCh37.p13 chr22: 30,214,392-30,214,447 ASCC2
    nsv5545244copy number variation1nstd206human GRCh38 chr22: 29,836,718-29,860,990 , GRCh37.p13 chr22: 30,232,707-30,256,979 ASCC2
    nsv5417376mobile element insertion1nstd206human GRCh38 chr22: 29,833,299-29,833,350 , GRCh37.p13 chr22: 30,229,288-30,229,339 ASCC2
    nsv5414003mobile element insertion1nstd206human GRCh38 chr22: 29,787,341-29,787,392 , GRCh37.p13 chr22: 30,183,330-30,183,381 ASCC2
    nsv5321178copy number variation1nstd204human GRCh38.p13 chr22: 29,677,880-29,826,306 , GRCh37.p13 chr22: 30,073,869-30,222,295 ASCC2, NF2, 3 more genes
    nsv5288578copy number variation1nstd204human GRCh38.p13 chr22: 29,677,801-29,826,300 , GRCh37.p13 chr22: 30,073,790-30,222,289 ASCC2, CABP7, 3 more genes
    nsv5287728copy number variation1nstd204human GRCh38.p13 chr22: 29,806,238-29,824,082 , GRCh37.p13 chr22: 30,202,227-30,220,071 ASCC2
    nsv5285928copy number variation1nstd204human GRCh38.p13 chr22: 29,818,983-29,821,782 , GRCh37.p13 chr22: 30,214,972-30,217,771 ASCC2
    nsv5285489copy number variation1nstd204human GRCh38.p13 chr22: 29,788,380-29,795,552 , GRCh37.p13 chr22: 30,184,369-30,191,541 ASCC2
    nsv5284088copy number variation1nstd204human GRCh38.p13 chr22: 29,786,480-29,825,997 , GRCh37.p13 chr22: 30,182,469-30,221,986 ASCC2
    nsv5284076copy number variation1nstd204human GRCh38.p13 chr22: 29,817,008-29,819,182 , GRCh37.p13 chr22: 30,212,997-30,215,171 ASCC2
    nsv5283602copy number variation1nstd204human GRCh38.p13 chr22: 29,813,658-29,816,757 , GRCh37.p13 chr22: 30,209,647-30,212,746 ASCC2
    nsv5281634copy number variation1nstd204human GRCh38.p13 chr22: 29,821,483-29,822,582 , GRCh37.p13 chr22: 30,217,472-30,218,571 ASCC2
    nsv5179058mobile element insertion1nstd203human GRCh38 chr22: 29,819,919-29,819,919 , GRCh37.p13 chr22: 30,215,908-30,215,908 ASCC2
    nsv5175631mobile element insertion1nstd203human GRCh38 chr22: 29,833,289-29,833,299 , GRCh37.p13 chr22: 30,229,278-30,229,288 ASCC2
    nsv5174317mobile element insertion1nstd203human GRCh38 chr22: 29,787,328-29,787,341 , GRCh37.p13 chr22: 30,183,317-30,183,330 ASCC2
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