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Items: 1 to 20 of 176

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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
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv7066406inversion1nstd229human GRCh38 chr12: 10,925,081-12,847,121 , GRCh37.p13 chr12: 11,077,680-13,000,055 RPL19P17, TAS2R64P, 56 more genes
    nsv7064789inversion1nstd229human GRCh38 chr12: 10,249,571-12,880,432 , GRCh37.p13 chr12: 10,402,170-13,033,366 DDX47, TAS2R64P, 89 more genes
    nsv7061545inversion1nstd229human GRCh38 chr12: 10,483,551-11,289,523 , GRCh37.p13 chr12: 10,636,150-11,442,457 TAS2R14, EIF2S3B, 40 more genes
    nsv6933892copy number variation1nstd229human GRCh38 chr12: 11,103,509-11,183,415 , GRCh37.p13 chr12: 11,256,108-11,336,017 TAS2R67P, TAS2R30, 5 more genes
    nsv6929092copy number variation1nstd229human GRCh38 chr12: 11,173,111-11,178,032 , GRCh37.p13 chr12: 11,325,710-11,330,631 TAS2R67P, SMIM10L1
    nsv6634456copy number variation1nstd102humanPathogenic GRCh37 chr12: 10,853,887-24,103,810 , GRCh38.p12 chr12: 10,701,288-23,950,876 TAS2R15P, LOC105369673, 209 more genes
    nsv6471659copy number variation1nstd223human GRCh38 chr12: 11,167,001-11,173,400 , GRCh37.p13 chr12: 11,319,600-11,325,999 PRH1, SMIM10L1, 2 more genes
    nsv6132720copy number variation1nstd213human GRCh37 chr12: 9,040,000-17,930,001 , GRCh38.p12 chr12: 8,887,404-17,777,067 A2M, A2MP1, 215 more genes
    nsv6132616copy number variation1nstd213human GRCh37 chr12: 8,100,000-12,900,001 , GRCh38.p12 chr12: 7,947,404-12,747,067 A2M, A2MP1, 178 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6132212copy number variation1nstd213human GRCh37 chr12: 10,670,000-12,390,001 , GRCh38.p12 chr12: 10,517,401-12,237,067 ETV6, LRP6, 57 more genes
    nsv6132138copy number variation1nstd213human GRCh37 chr12: 11,250,000-19,950,001 , GRCh38.p12 chr12: 11,097,401-19,797,067 ARHGDIB, ART4, 139 more genes
    nsv5345446translocation1nstd200human GRCh37 chr12: 11,327,495-11,327,495 , GRCh37 chr12: 11,327,441-11,327,441 , GRCh38.p12 chr12: 11,174,842-11,174,842 , GRCh38.p12 chr12: 11,174,896-11,174,896 , GRCh38.p12 chr12|NT_187658.1: 369,837-369,837 , GRCh38.p12 chr12|NT_187658.1: 369,783-369,783 , GRCh38.p12 chr12|NW_003571050.1: 405,496-405,496 , GRCh38.p12 chr12|NW_003571050.1: 405,550-405,550 SMIM10L1
    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
    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
    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
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