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Items: 1 to 20 of 160

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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
    nsv5972780inversion1nstd209human GRCh38 chr12: 10,984,398-10,992,044 , GRCh37.p13 chr12: 11,136,997-11,144,643 PRH1, TAS2R50, 2 more genes
    nsv5910757copy number variation1nstd209human GRCh38 chr12: 10,984,405-10,989,244 , GRCh37.p13 chr12: 11,137,004-11,141,843 PRH1, TAS2R50, 2 more genes
    nsv5856942copy number variation1nstd209human GRCh38 chr12: 10,984,521-10,989,045 , GRCh37.p13 chr12: 11,137,120-11,141,644 PRH1-TAS2R14, TAS2R50, 2 more genes
    nsv5848824copy number variation2nstd209human GRCh38 chr12: 10,986,221-10,987,220 , GRCh37.p13 chr12: 11,138,820-11,139,819 PRH1, PRH1-PRR4, 2 more genes
    nsv5511203copy number variation1nstd206human GRCh38 chr12: 10,984,355-10,989,286 , GRCh37.p13 chr12: 11,136,954-11,141,885 TAS2R50, PRH1-TAS2R14, 2 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
    nsv5321949translocation1nstd204human GRCh38.p13 chr12: 10,984,400-10,984,400 , GRCh38.p13 chr12: 10,992,045-10,992,045 , GRCh37.p13 chr12: 11,136,999-11,136,999 , GRCh37.p13 chr12: 11,144,644-11,144,644 PRH1, TAS2R50, 2 more genes
    nsv5305202copy number variation1nstd204human GRCh37.p13 chr12: 11,136,988-11,141,849 , GRCh38.p13 chr12: 10,984,389-10,989,250 PRH1, TAS2R50, 2 more genes
    nsv5269244copy number variation1nstd204human GRCh38.p13 chr12: 10,984,446-10,989,395 , GRCh37.p13 chr12: 11,137,045-11,141,994 PRH1-PRR4, TAS2R50, 2 more genes
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4840654copy number variation1nstd200human GRCh37 chr12: 11,136,991-11,141,853 , GRCh38.p12 chr12: 10,984,392-10,989,254 , GRCh38.p12 chr12|NT_187658.1: 183,085-187,947 , GRCh38.p12 chr12|NW_003571050.1: 183,098-187,960 PRH1-TAS2R14, PRH1-PRR4, 2 more genes
    nsv4708101tandem duplication1nstd195human GRCh37 chr12: 11,139,922-11,139,923 , GRCh38.p12 chr12: 10,987,323-10,987,324 , GRCh38.p12 chr12|NT_187658.1: 186,016-186,017 , GRCh38.p12 chr12|NW_003571050.1: 186,029-186,030 PRH1, TAS2R50, 2 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
    nsv4601539copy number variation1nstd183human GRCh37 chr12: 11,060,990-11,504,091 , GRCh38.p12 chr12|NT_187658.1: 107,097-546,120 , GRCh38.p12 chr12|NW_003571050.1: 107,097-408,271 , GRCh38.p12 chr12: 10,908,391-11,351,157 , TAS2R64P, 26 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
    nsv4421859copy number variation1nstd174human GRCh37 chr12: 11,133,432-11,231,459 , GRCh38.p12 chr12|NW_003571050.1: 179,539-277,566 , GRCh38.p12 chr12|NT_187658.1: 179,530-279,969 , GRCh38.p12 chr12: 10,980,833-11,078,860 TAS2R63P, TAS2R46, 9 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
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