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Items: 1 to 20 of 139

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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
    nsv7076490inversion1nstd229human GRCh38 chr12: 20,940,376-25,948,754 , GRCh37.p13 chr12: 21,093,310-26,101,687 LOC102724261, IRAG2, 59 more genes
    nsv7070485inversion1nstd229human GRCh38 chr12: 21,009,516-22,041,867 , GRCh37.p13 chr12: 21,162,450-22,194,801 SLCO1B3-SLCO1B7, SPX, 15 more genes
    nsv7068678inversion1nstd229human GRCh38 chr12: 20,996,324-22,051,286 , GRCh37.p13 chr12: 21,149,258-22,204,220 SLCO1B3-SLCO1B7, ABCC9, 16 more genes
    nsv6930201copy number variation1nstd229human GRCh38 chr12: 22,003,001-22,013,000 , GRCh37.p13 chr12: 22,155,935-22,165,934 THEM4P1
    nsv6922372copy number variation1nstd229human GRCh38 chr12: 22,007,555-22,020,953 , GRCh37.p13 chr12: 22,160,489-22,173,887 THEM4P1
    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
    nsv6314083copy number variation1nstd102humanPathogenic GRCh37 chr12: 17,884,992-26,704,895 , GRCh38.p12 chr12: 17,732,058-26,551,962 SLCO1B1, RERGL, 105 more genes
    nsv6132682copy number variation1nstd213human GRCh37 chr12: 21,790,000-22,520,001 , GRCh38.p12 chr12: 21,637,066-22,367,067 KCNJ8, LDHB, 11 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6132231copy number variation1nstd213human GRCh37 chr12: 21,890,000-23,190,001 , GRCh38.p12 chr12: 21,737,066-23,037,067 C2CD5, C2CD5-AS1, 18 more genes
    nsv6132229copy number variation1nstd213human GRCh37 chr12: 20,940,000-22,650,001 , GRCh38.p12 chr12: 20,787,066-22,497,067 GYS2, IAPP, 24 more genes
    nsv5980132inversion1nstd209human GRCh38 chr12: 21,873,888-24,109,273 , GRCh37.p13 chr12: 22,026,822-24,262,207 , ST8SIA1, 19 more genes
    nsv5923742copy number variation1nstd209human GRCh38 chr12: 21,398,810-28,763,815 , GRCh37.p13 chr12: 21,551,744-28,916,748 , LOC105369710, 101 more genes
    nsv5916901copy number variation1nstd209human GRCh38 chr12: 21,398,719-28,763,765 , GRCh37.p13 chr12: 21,551,653-28,916,698 , LOC105369704, 101 more genes
    nsv4729730copy number variation1nstd102humanPathogenic GRCh37 chr12: 21,582,333-24,920,271 , GRCh38.p12 chr12: 21,429,399-24,767,337 CMAS, ETNK1-DT, 34 more genes
    nsv4704446copy number variation1nstd195human GRCh37 chr12: 22,130,901-22,289,551 , GRCh38.p12 chr12: 21,977,967-22,136,617 CMAS, THEM4P1, 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
    nsv4615807copy number variation1nstd183human GRCh37 chr12: 21,992,936-22,367,512 , GRCh38.p12 chr12: 21,840,002-22,214,578 ST8SIA1, ABCC9, 5 more genes
    nsv4456793copy number variation1nstd102humanPathogenic GRCh37 chr12: 16,141,429-27,733,325 , GRCh38.p12 chr12: 15,988,495-27,580,392 PDE3A, ETFRF1, 133 more genes
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