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Items: 1 to 20 of 142

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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
    nsv5494258copy number variation1nstd206human GRCh38 chr12: 10,925,220-10,950,133 , GRCh37.p13 chr12: 11,077,819-11,102,732 PRH2, PRH1-PRR4, 3 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
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4972220copy number variation1nstd200human GRCh38 chr12: 10,925,220-10,950,133 , GRCh37.p13 chr12: 11,077,819-11,102,732 PRH2, PRH1-TAS2R14, 3 more genes
    nsv4972213copy number variation1nstd200human GRCh38 chr12: 10,818,580-10,950,616 , GRCh37.p13 chr12: 10,971,179-11,103,215 , TAS2R12P, 9 more genes
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4834111copy number variation1nstd200human GRCh37 chr12: 10,971,179-11,103,215 , GRCh38.p12 chr12|NW_003571050.1: 17,286-149,322 , GRCh38.p12 chr12: 10,818,580-10,950,616 , GRCh38.p12 chr12|NT_187658.1: 17,286-149,322 , PRH1-TAS2R14, 9 more genes
    nsv4832662copy number variation1nstd200human GRCh37 chr12: 11,077,819-11,102,732 , GRCh38.p12 chr12|NW_003571050.1: 123,926-148,839 , GRCh38.p12 chr12: 10,925,220-10,950,133 , GRCh38.p12 chr12|NT_187658.1: 123,926-148,839 PRH2, PRH1-TAS2R14, 3 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
    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
    nsv4211102copy number variation1nstd166human GRCh37.p13 chr12: 11,077,819-11,102,732 , GRCh38.p12 chr12|NT_187658.1: 123,926-148,839 , GRCh38.p12 chr12|NW_003571050.1: 123,926-148,839 , GRCh38.p12 chr12: 10,925,220-10,950,133 PRH2, PRH1-PRR4, 3 more genes
    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
    nsv3922178copy number variation1nstd102humanPathogenic GRCh37 chr12: 2,980,907-15,140,282 , NCBI36 chr12: 2,851,168-15,031,549 , GRCh38 chr12: 2,871,741-14,987,348 H2AJ, GPR162, 378 more genes
    nsv3919557copy number variation1nstd102humanPathogenic NCBI36 chr12: 59,934-11,147,715 , GRCh37.p13 chr12: 189,673-11,256,448 , GRCh38.p12 chr12: 80,507-11,103,849 ING4, LINC02827, 350 more genes
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