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Items: 1 to 20 of 829

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7077542inversion1nstd229human GRCh38 chr12: 7,565,102-9,354,075 , GRCh37.p13 chr12: 7,717,698-9,506,671 ALG1L10P, RPL15P17, 69 more genes
    nsv7074732inversion1nstd229human GRCh38 chr12: 9,199,258-9,594,738 , GRCh37.p13 chr12: 9,351,854-9,747,334 KLRB1, PZP, 14 more genes
    nsv7072287inversion1nstd229human GRCh38 chr12: 9,193,237-9,208,152 , GRCh37.p13 chr12: 9,345,833-9,360,748 PZP, KLRG1
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv7072108inversion1nstd229human GRCh38 chr12: 9,111,990-9,112,090 , GRCh37.p13 chr12: 9,264,586-9,264,686 KLRG1, A2M
    nsv7068023inversion1nstd229human GRCh38 chr12: 8,672,182-8,987,980 , GRCh37.p13 chr12: 8,824,778-9,140,576 M6PR, KLRG1, 5 more genes
    nsv7068010inversion1nstd229human GRCh38 chr12: 7,025,778-10,225,656 , GRCh37.p13 chr12: 7,178,850-10,378,255 GOT2P3, CLEC2B, 123 more genes
    nsv7066301inversion1nstd229human GRCh38 chr12: 9,127,395-9,189,622 , GRCh37.p13 chr12: 9,279,991-9,342,218 PZP, BTG1P1, 3 more genes
    nsv7065364inversion1nstd229human GRCh38 chr12: 9,198,710-9,372,424 , GRCh37.p13 chr12: 9,351,306-9,525,020 PZP, PTMAP4, 8 more genes
    nsv7064008inversion1nstd229human GRCh38 chr12: 6,716,253-10,225,825 , GRCh37.p13 chr12: 6,825,419-10,378,424 PTMAP4, COPS7A, 153 more genes
    nsv7061199inversion1nstd229human GRCh38 chr12: 9,195,951-9,208,602 , GRCh37.p13 chr12: 9,348,547-9,361,198 PZP, KLRG1
    nsv7059773inversion1nstd229human GRCh38 chr12: 8,963,554-9,585,969 , GRCh37.p13 chr12: 9,116,150-9,738,565 DDX12P, LOC105369647, 20 more genes
    nsv6937671copy number variation1nstd229human GRCh38 chr12: 9,184,963-9,212,181 , GRCh37.p13 chr12: 9,337,559-9,364,777 PZP, KLRG1
    nsv6937066copy number variation1nstd229human GRCh38 chr12: 8,976,401-8,980,300 , GRCh37.p13 chr12: 9,128,997-9,132,896 KLRG1
    nsv6936598copy number variation1nstd229human GRCh38 chr12: 8,996,032-9,000,203 , GRCh37.p13 chr12: 9,148,628-9,152,799 KLRG1
    nsv6935327copy number variation1nstd229human GRCh38 chr12: 9,182,020-9,187,933 , GRCh37.p13 chr12: 9,334,616-9,340,529 KLRG1, PZP
    nsv6935299copy number variation1nstd229human GRCh38 chr12: 9,193,326-9,216,362 , GRCh37.p13 chr12: 9,345,922-9,368,958 KLRG1, PZP
    nsv6935262copy number variation1nstd229human GRCh38 chr12: 9,069,701-9,079,900 , GRCh37.p13 chr12: 9,222,297-9,232,496 KLRG1, A2M
    nsv6933589copy number variation1nstd229human GRCh38 chr12: 8,998,901-9,003,100 , GRCh37.p13 chr12: 9,151,497-9,155,696 KLRG1
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