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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097148copy number variation1nstd102humanPathogenic GRCh37 chr5: 52,285,299-56,189,507 , GRCh38.p12 chr5: 52,989,469-56,893,680 RPL37P25, CCNO, 69 more genes
    nsv7057901inversion1nstd229human GRCh38 chr5: 53,201,194-56,162,991 , GRCh37.p13 chr5: 52,497,024-55,458,818 , PLPP1, 55 more genes
    nsv7057647inversion1nstd229human GRCh38 chr5: 54,827,303-54,827,360 , GRCh37.p13 chr5: 54,123,131-54,123,188 CSPG4BP
    nsv7056130inversion1nstd229human GRCh38 chr5: 53,218,622-56,162,980 , GRCh37.p13 chr5: 52,514,452-55,458,807 , ASS1P9, 54 more genes
    nsv7053769inversion1nstd229human GRCh38 chr5: 54,829,597-54,833,225 , GRCh37.p13 chr5: 54,125,425-54,129,053 CSPG4BP
    nsv7041530inversion1nstd229human GRCh38 chr5: 54,841,193-54,852,864 , GRCh37.p13 chr5: 54,137,021-54,148,692 CSPG4BP
    nsv6772087copy number variation1nstd229human GRCh38 chr5: 54,814,801-54,826,500 , GRCh37.p13 chr5: 54,110,629-54,122,328 CSPG4BP
    nsv6770601copy number variation1nstd229human GRCh38 chr5: 54,814,701-54,826,700 , GRCh37.p13 chr5: 54,110,529-54,122,528 CSPG4BP
    nsv6768428copy number variation1nstd229human GRCh38 chr5: 54,813,601-54,825,500 , GRCh37.p13 chr5: 54,109,429-54,121,328 CSPG4BP
    nsv6766352copy number variation1nstd229human GRCh38 chr5: 52,086,933-59,394,572 , GRCh37.p13 chr5: 51,382,767-58,690,398 , LOC105378980, 102 more genes
    nsv6766214copy number variation1nstd229human GRCh38 chr5: 54,814,729-54,825,504 , GRCh37.p13 chr5: 54,110,557-54,121,332 CSPG4BP
    nsv6765828copy number variation1nstd229human GRCh38 chr5: 54,808,493-54,809,040 , GRCh37.p13 chr5: 54,104,321-54,104,868 CSPG4BP
    nsv6765290copy number variation1nstd229human GRCh38 chr5: 54,824,133-54,824,514 , GRCh37.p13 chr5: 54,119,961-54,120,342 CSPG4BP
    nsv6763689copy number variation1nstd229human GRCh38 chr5: 54,834,586-54,844,258 , GRCh37.p13 chr5: 54,130,414-54,140,086 CSPG4BP
    nsv6762484copy number variation1nstd229human GRCh38 chr5: 54,813,401-54,825,600 , GRCh37.p13 chr5: 54,109,229-54,121,428 CSPG4BP
    nsv6571603inversion1nstd223human GRCh38 chr5: 54,841,193-54,852,864 , GRCh37.p13 chr5: 54,137,021-54,148,692 CSPG4BP
    nsv6409965copy number variation1nstd223human GRCh38 chr5: 54,807,101-54,808,200 , GRCh37.p13 chr5: 54,102,929-54,104,028 CSPG4BP
    nsv6408542copy number variation1nstd223human GRCh38 chr5: 54,807,501-54,813,900 , GRCh37.p13 chr5: 54,103,329-54,109,728 CSPG4BP
    nsv6405398copy number variation1nstd223human GRCh38 chr5: 54,818,901-54,825,200 , GRCh37.p13 chr5: 54,114,729-54,121,028 CSPG4BP
    nsv6399321copy number variation1nstd223human GRCh38 chr5: 54,834,586-54,844,254 , GRCh37.p13 chr5: 54,130,414-54,140,082 CSPG4BP
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