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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6937959copy number variation1nstd229human GRCh38 chr12: 48,931,090-48,935,070 , GRCh37.p13 chr12: 49,324,873-49,328,853 ARF3
    nsv6937357copy number variation1nstd229human GRCh38 chr12: 48,930,815-48,934,567 , GRCh37.p13 chr12: 49,324,598-49,328,350 ARF3
    nsv6927701copy number variation1nstd229human GRCh38 chr12: 48,930,672-48,930,725 , GRCh37.p13 chr12: 49,324,455-49,324,508 ARF3
    nsv6472380copy number variation1nstd223human GRCh38 chr12: 48,931,090-48,935,070 , GRCh37.p13 chr12: 49,324,873-49,328,853 ARF3
    nsv6458409copy number variation1nstd223human GRCh38 chr12: 48,919,052-48,941,049 , GRCh37.p13 chr12: 49,312,835-49,334,832 CCDC65, FKBP11, 1 more genes
    nsv6458293copy number variation1nstd223human GRCh38 chr12: 48,942,873-48,945,346 , GRCh37.p13 chr12: 49,336,656-49,339,129 ARF3
    nsv6307139copy number variation1nstd186human GRCh37 chr12: 49,325,065-49,325,119 , GRCh38.p12 chr12: 48,931,282-48,931,336 ARF3
    nsv6305859copy number variation1nstd186human GRCh37 chr12: 49,332,894-49,333,436 , GRCh38.p12 chr12: 48,939,111-48,939,653 ARF3
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132595copy number variation1nstd213human GRCh37 chr12: 49,290,000-49,380,001 , GRCh38.p12 chr12: 48,896,217-48,986,218 ARF3, WNT1, 7 more genes
    nsv5564512copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 37,873,948-49,578,619 , GRCh38.p12 chr12: 37,480,146-49,184,836 ADCY6, ABCD2, 187 more genes
    nsv5498430copy number variation1nstd206human GRCh38 chr12: 48,940,108-48,940,946 , GRCh37.p13 chr12: 49,333,891-49,334,729 ARF3
    nsv5498293copy number variation1nstd206human GRCh38 chr12: 48,931,282-48,931,336 , GRCh37.p13 chr12: 49,325,065-49,325,119 ARF3
    nsv5496313copy number variation1nstd206human GRCh38 chr12: 48,947,571-48,948,181 , GRCh37.p13 chr12: 49,341,354-49,341,964 ARF3
    nsv5495996copy number variation1nstd206human GRCh38 chr12: 48,939,781-48,939,995 , GRCh37.p13 chr12: 49,333,564-49,333,778 ARF3
    nsv5494974copy number variation1nstd206human GRCh38 chr12: 48,939,111-48,939,653 , GRCh37.p13 chr12: 49,332,894-49,333,436 ARF3
    nsv5122945mobile element insertion1nstd203human GRCh38 chr12: 48,928,583-48,928,623 , GRCh37.p13 chr12: 49,322,366-49,322,406 ARF3
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv4985564copy number variation1nstd200human GRCh38 chr12: 48,945,556-48,948,817 , GRCh37.p13 chr12: 49,339,339-49,342,600 ARF3
    nsv4985563copy number variation1nstd200human GRCh38 chr12: 48,919,052-48,941,049 , GRCh37.p13 chr12: 49,312,835-49,334,832 ARF3, FKBP11, 1 more genes
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