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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074641inversion1nstd229human GRCh38 chr12: 52,659,002-59,632,575 , GRCh37.p13 chr12: 53,052,786-60,026,356 , LOC105369777, 292 more genes
    nsv7069901inversion1nstd229human GRCh38 chr12: 51,176,082-54,825,440 , GRCh37.p13 chr12: 51,569,865-55,219,224 , HOXC5, 158 more genes
    nsv6937548copy number variation1nstd229human GRCh38 chr12: 54,280,153-54,280,525 , GRCh37.p13 chr12: 54,673,937-54,674,309 HNRNPA1, CBX5
    nsv6934687copy number variation1nstd229human GRCh38 chr12: 54,271,998-54,275,733 , GRCh37.p13 chr12: 54,665,782-54,669,517 SCAT2, CBX5
    nsv6928573copy number variation1nstd229human GRCh38 chr12: 54,235,367-54,238,078 , GRCh37.p13 chr12: 54,629,151-54,631,862 CBX5
    nsv6592274inversion1nstd223human GRCh38 chr12: 54,261,047-54,261,586 , GRCh37.p13 chr12: 54,654,831-54,655,370 SCAT2, CBX5
    nsv6586839inversion1nstd223human GRCh38 chr12: 54,274,801-54,275,495 , GRCh37.p13 chr12: 54,668,585-54,669,279 SCAT2, CBX5
    nsv6582258inversion1nstd223human GRCh38 chr12: 54,243,733-54,244,306 , GRCh37.p13 chr12: 54,637,517-54,638,090 CBX5
    nsv6578363inversion1nstd223human GRCh38 chr12: 54,260,918-54,261,586 , GRCh37.p13 chr12: 54,654,702-54,655,370 SCAT2, CBX5
    nsv6467013copy number variation1nstd223human GRCh38 chr12: 54,266,400-54,268,105 , GRCh37.p13 chr12: 54,660,184-54,661,889 CBX5, SCAT2
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132426copy number variation1nstd213human GRCh37 chr12: 52,740,000-55,260,001 , GRCh38.p12 chr12: 52,346,216-54,866,217 , HOXC4, 122 more genes
    nsv5866777copy number variation1nstd209human GRCh38 chr12: 54,265,948-54,267,147 , GRCh37.p13 chr12: 54,659,732-54,660,931 CBX5, SCAT2
    nsv5713492mobile element insertion2nstd211human GRCh38 chr12: 54,238,566-54,238,566 , GRCh37.p13 chr12: 54,632,350-54,632,350 CBX5
    nsv5513905copy number variation1nstd206human GRCh38 chr12: 54,280,128-54,356,128 , GRCh37.p13 chr12: 54,673,912-54,749,912 HNRNPA1, NFE2, 6 more genes
    nsv5505642copy number variation1nstd206human GRCh38 chr12: 54,249,854-54,250,598 , GRCh37.p13 chr12: 54,643,638-54,644,382 CBX5
    nsv5431463mobile element insertion1nstd206human GRCh38 chr12: 54,238,566-54,238,576 , GRCh37.p13 chr12: 54,632,350-54,632,360 CBX5
    nsv5131035mobile element insertion1nstd203human GRCh38 chr12: 54,233,765-54,233,777 , GRCh37.p13 chr12: 54,627,549-54,627,561 CBX5
    nsv5125256mobile element insertion1nstd203human GRCh38 chr12: 54,241,266-54,241,280 , GRCh37.p13 chr12: 54,635,050-54,635,064 CBX5
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
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