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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099193copy number variation1nstd231human GRCh38.p12 chr1: 32,456,017-38,905,781 , GRCh37 chr1: 32,921,618-39,371,453 AK2, COL8A2, 151 more genes
    nsv7046389inversion1nstd229human GRCh38 chr1: 31,492,639-36,569,102 , GRCh37.p13 chr1: 32,017,064-37,034,703 LOC105378642, TMEM35B, 127 more genes
    nsv6649163copy number variation1nstd229human GRCh38 chr1: 33,852,479-33,859,933 , GRCh37.p13 chr1: 34,318,080-34,325,534 HMGB4, CSMD2
    nsv6328322copy number variation1nstd223human GRCh38 chr1: 33,404,224-33,959,487 , GRCh37.p13 chr1: 33,869,825-34,425,088 HSPD1P14, CSMD2, 5 more genes
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
    nsv6225602insertion1nstd214human GRCh38 chr1: 33,864,353-33,864,353 , GRCh37.p13 chr1: 34,329,954-34,329,954 CSMD2, HMGB4
    nsv6133869copy number variation1nstd213human GRCh37 chr1: 33,400,000-36,950,001 , GRCh38.p12 chr1: 32,934,399-36,484,400 AK2, COL8A2, 77 more genes
    nsv6052652insertion1nstd212human GRCh38 chr1: 33,864,929-33,864,929 , GRCh37.p13 chr1: 34,330,530-34,330,530 CSMD2, HMGB4
    nsv5963365insertion1nstd209human GRCh38 chr1: 33,862,822-33,862,822 , GRCh37.p13 chr1: 34,328,423-34,328,423 CSMD2, HMGB4
    nsv5879583copy number variation1nstd209human GRCh38 chr1: 33,859,807-33,861,906 , GRCh37.p13 chr1: 34,325,408-34,327,507 CSMD2, HMGB4
    nsv5877941copy number variation1nstd209human GRCh38 chr1: 33,861,907-33,862,817 , GRCh37.p13 chr1: 34,327,508-34,328,418 HMGB4, CSMD2
    nsv5871911copy number variation1nstd209human GRCh38 chr1: 33,859,906-33,862,821 , GRCh37.p13 chr1: 34,325,507-34,328,422 CSMD2, HMGB4
    nsv5616740insertion1nstd207human GRCh38 chr1: 33,864,929-33,864,929 , GRCh37.p13 chr1: 34,330,530-34,330,530 HMGB4, CSMD2
    nsv5430763copy number variation1nstd206human GRCh38 chr1: 33,852,479-33,859,939 , GRCh37.p13 chr1: 34,318,080-34,325,540 CSMD2, HMGB4
    nsv5419855copy number variation1nstd206human GRCh38 chr1: 33,404,224-33,959,490 , GRCh37.p13 chr1: 33,869,825-34,425,091 , ZSCAN20, 6 more genes
    nsv4903343copy number variation1nstd200human GRCh38 chr1: 33,404,224-33,959,490 , GRCh37.p13 chr1: 33,869,825-34,425,091 , CSMD2-AS1, 6 more genes
    nsv4780770copy number variation1nstd200human GRCh37 chr1: 33,869,825-34,425,091 , GRCh38.p12 chr1: 33,404,224-33,959,490 , LOC100422287, 6 more genes
    nsv4773009copy number variation1nstd200human GRCh37 chr1: 34,327,497-34,328,433 , GRCh38.p12 chr1: 33,861,896-33,862,832 HMGB4, CSMD2
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4763445insertion1nstd199human GRCh37 chr1: 34,330,469-34,330,469 , GRCh38.p12 chr1: 33,864,868-33,864,868 CSMD2, HMGB4
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