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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4835868copy number variation1nstd200human GRCh37 chr12: 49,344,625-49,344,931 , GRCh38.p12 chr12: 48,950,842-48,951,148 ARF3
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4728793copy number variation1nstd102humanUncertain significance GRCh37 chr12: 49,024,019-50,299,974 , GRCh38.p12 chr12: 48,630,236-49,906,191 SPATS2, SPMIP11, 62 more genes
    nsv4578649copy number variation1nstd102humanPathogenic GRCh37 chr12: 49,034,325-49,468,966 , GRCh38.p12 chr12: 48,640,542-49,075,183 WNT1, SPMIP11, 29 more genes
    nsv4500176mobile element insertion1nstd166human GRCh37.p13 chr12: 49,348,919-49,348,919 , GRCh38.p12 chr12: 48,955,136-48,955,136 ARF3
    nsv4330649inversion1nstd166human GRCh37.p13 chr12: 49,327,598-49,328,536 , GRCh38.p12 chr12: 48,933,815-48,934,753 ARF3
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
    nsv4210927copy number variation1nstd166human GRCh37.p13 chr12: 49,332,894-49,333,436 , GRCh38.p12 chr12: 48,939,111-48,939,653 ARF3
    nsv3920847inversion1nstd102humanUncertain significance GRCh38.p12 chr12: 26,217,318-53,967,754 , GRCh37 chr12: 26,370,251-54,361,538 , ASIC1, 491 more genes
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