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Items: 1 to 20 of 146

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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
    nsv5505186copy number variation1nstd206human GRCh38 chr12: 10,720,422-10,881,006 , GRCh37.p13 chr12: 10,873,021-11,033,605 , LINC02366, 11 more genes
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5267073copy number variation1nstd204human GRCh38.p13 chr12: 10,758,701-10,763,400 , GRCh37.p13 chr12: 10,911,300-10,915,999 LINC02366
    nsv5181747mobile element insertion1nstd203human GRCh38 chr12: 10,771,058-10,771,072 , GRCh37.p13 chr12: 10,923,657-10,923,671 HSPE1P12, LINC02366
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4974341copy number variation1nstd200human GRCh38 chr12: 10,720,422-10,881,006 , GRCh37.p13 chr12: 10,873,021-11,033,605 , HSPE1P12, 11 more genes
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4673236copy number variation1nstd186human GRCh37 chr12: 10,912,510-10,924,167 , GRCh38.p12 chr12: 10,759,911-10,771,568 HSPE1P12, LINC02366
    nsv4604287copy number variation1nstd183human GRCh37 chr12: 10,912,510-10,924,167 , GRCh38.p12 chr12: 10,759,911-10,771,568 LINC02366, HSPE1P12
    nsv4602865copy number variation1nstd183human GRCh37 chr12: 10,910,786-10,954,396 , GRCh38.p12 chr12: 10,758,187-10,801,797 TAS2R7, HSPE1P12, 1 more genes
    nsv4506994mobile element insertion1nstd166human GRCh37.p13 chr12: 10,902,411-10,902,411 , GRCh38.p12 chr12: 10,749,812-10,749,812 LINC02366
    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
    nsv4324171inversion1nstd166human GRCh37.p13 chr12: 6,338,819-22,046,498 , GRCh38.p12 chr12: 6,229,653-21,893,564 , APOBEC1, 414 more genes
    nsv4200302copy number variation1nstd166human GRCh37.p13 chr12: 10,897,800-10,902,144 , GRCh38.p12 chr12: 10,745,201-10,749,545 LINC02366
    nsv3924262copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,835,837 , GRCh38 chr12: 64,620-34,682,902 , NCBI36 chr12: 44,047-34,727,104 ENO2, SLC6A13, 684 more genes
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