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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976275inversion1nstd209human GRCh38 chr12: 10,296,446-11,054,973 , GRCh37.p13 chr12: 10,449,045-11,207,572 , KLRC1, 40 more genes
    nsv5971846insertion1nstd209human GRCh38 chr12: 10,334,174-10,334,174 , GRCh37.p13 chr12: 10,486,773-10,486,773 LINC02617
    nsv5909649copy number variation1nstd209human GRCh38 chr12: 10,331,193-10,331,418 , GRCh37.p13 chr12: 10,483,792-10,484,017 LINC02617
    nsv5848145copy number variation2nstd209human GRCh38 chr12: 10,336,577-10,338,078 , GRCh37.p13 chr12: 10,489,176-10,490,677 LINC02617
    nsv5715162mobile element insertion1nstd211human GRCh38 chr12: 10,332,766-10,332,766 , GRCh37.p13 chr12: 10,485,365-10,485,365 LINC02617
    nsv5658109insertion1nstd207human GRCh38 chr12: 10,334,173-10,334,173 , GRCh37.p13 chr12: 10,486,772-10,486,772 LINC02617
    nsv5590829copy number variation1nstd207human GRCh38 chr12: 10,337,315-10,338,027 , GRCh37.p13 chr12: 10,489,914-10,490,626 LINC02617
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5280044copy number variation1nstd204human GRCh38.p13 chr12: 10,336,601-10,338,100 , GRCh37.p13 chr12: 10,489,200-10,490,699 LINC02617
    nsv5273438copy number variation1nstd204human GRCh38.p13 chr12: 10,336,527-10,337,755 , GRCh37.p13 chr12: 10,489,126-10,490,354 LINC02617
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4972197copy number variation1nstd200human GRCh38 chr12: 10,333,090-10,338,228 , GRCh37.p13 chr12: 10,485,689-10,490,827 LINC02617
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4838399copy number variation1nstd200human GRCh37 chr12: 10,485,689-10,490,827 , GRCh38.p12 chr12: 10,333,090-10,338,228 LINC02617
    nsv4754500insertion1nstd199human GRCh37 chr12: 10,486,768-10,486,768 , GRCh38.p12 chr12: 10,334,169-10,334,169 LINC02617
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
    nsv4436324complex substitution1nstd102humanUncertain significance GRCh38.p12 chr12: 9,922,177-18,648,019 , GRCh37 chr12: 10,074,776-18,800,953 ARHGDIB, ART4, 181 more genes
    nsv4350818copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,216-15,001,420 , GRCh38.p12 chr12: 80,050-14,848,486 LOC107984495, KLRC1, 432 more genes
    nsv4350159copy number variation1nstd102humanPathogenic GRCh37 chr12: 10,336,209-13,535,349 , GRCh38.p12 chr12: 10,183,610-13,382,415 CREBL2, TAS2R18P, 103 more genes
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