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Items: 1 to 20 of 389

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137099copy number variation1nstd102humanPathogenic GRCh37 chr12: 11,463,270-14,019,142 , GRCh38.p12 chr12: 11,310,336-13,866,208 HTR7P1, RPL37AP9, 55 more genes
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7077114inversion1nstd229human GRCh38 chr12: 11,615,098-12,052,126 , GRCh37.p13 chr12: 11,768,032-12,205,060 ETV6, BCL2L14
    nsv7071195inversion1nstd229human GRCh38 chr12: 11,970,486-12,128,407 , GRCh37.p13 chr12: 12,123,420-12,281,341 PTMAP9, BCL2L14, 2 more genes
    nsv7066406inversion1nstd229human GRCh38 chr12: 10,925,081-12,847,121 , GRCh37.p13 chr12: 11,077,680-13,000,055 RPL19P17, TAS2R64P, 56 more genes
    nsv7064789inversion1nstd229human GRCh38 chr12: 10,249,571-12,880,432 , GRCh37.p13 chr12: 10,402,170-13,033,366 DDX47, TAS2R64P, 89 more genes
    nsv7064011inversion1nstd229human GRCh38 chr12: 11,255,910-17,864,916 , GRCh37.p13 chr12: 11,408,826-18,017,850 MGP, MIR3974, 108 more genes
    nsv6936746copy number variation1nstd229human GRCh38 chr12: 12,079,801-12,081,800 , GRCh37.p13 chr12: 12,232,735-12,234,734 BCL2L14
    nsv6933974copy number variation1nstd229human GRCh38 chr12: 12,099,895-12,101,714 , GRCh37.p13 chr12: 12,252,829-12,254,648 BCL2L14
    nsv6927721copy number variation1nstd229human GRCh38 chr12: 12,089,408-12,094,998 , GRCh37.p13 chr12: 12,242,342-12,247,932 BCL2L14
    nsv6924167copy number variation1nstd229human GRCh38 chr12: 11,980,192-12,049,609 , GRCh37.p13 chr12: 12,133,126-12,202,543 BCL2L14
    nsv6920344copy number variation1nstd229human GRCh38 chr12: 12,037,067-12,124,936 , GRCh37.p13 chr12: 12,190,001-12,277,870 MIR1244-4, LRP6, 2 more genes
    nsv6919393copy number variation1nstd229human GRCh38 chr12: 12,068,188-12,085,007 , GRCh37.p13 chr12: 12,221,122-12,237,941 BCL2L14
    nsv6918396copy number variation1nstd229human GRCh38 chr12: 12,093,853-12,098,425 , GRCh37.p13 chr12: 12,246,787-12,251,359 BCL2L14
    nsv6634456copy number variation1nstd102humanPathogenic GRCh37 chr12: 10,853,887-24,103,810 , GRCh38.p12 chr12: 10,701,288-23,950,876 TAS2R15P, LOC105369673, 209 more genes
    nsv6469181copy number variation1nstd223human GRCh38 chr12: 12,099,893-12,101,712 , GRCh37.p13 chr12: 12,252,827-12,254,646 BCL2L14
    nsv6468113copy number variation1nstd223human GRCh38 chr12: 12,058,591-12,063,789 , GRCh37.p13 chr12: 12,211,525-12,216,723 BCL2L14
    nsv6462946copy number variation1nstd223human GRCh38 chr12: 12,079,984-12,080,922 , GRCh37.p13 chr12: 12,232,918-12,233,856 BCL2L14
    nsv6309465copy number variation2nstd102humanUncertain significance GRCh37 chr12: 11,803,062-15,835,885 , GRCh38.p12 chr12: 11,650,128-15,682,951 LRP6, APOLD1, 78 more genes
    nsv6240669mobile element insertion1nstd215human GRCh38 chr12: 12,050,762-12,050,762 , GRCh37.p13 chr12: 12,203,696-12,203,696 BCL2L14
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