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Items: 1 to 20 of 226

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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
    nsv7093966copy number variation1nstd102humanUncertain significance GRCh37 chr12: 20,522,219-22,089,608 , GRCh38.p12 chr12: 20,369,285-21,936,674 LOC728688, SPX, 19 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
    nsv7068185inversion1nstd229human GRCh38 chr12: 20,036,076-21,999,484 , GRCh37.p13 chr12: 20,189,010-22,152,418 UBE2L2, RECQL, 25 more genes
    nsv7063671inversion1nstd229human GRCh38 chr12: 20,030,237-21,994,711 , GRCh37.p13 chr12: 20,183,171-22,147,645 SLCO1B3-SLCO1B7, LINC02468, 25 more genes
    nsv7060644inversion1nstd229human GRCh38 chr12: 20,030,249-21,999,483 , GRCh37.p13 chr12: 20,183,183-22,152,417 SLCO1B3-SLCO1B7, SLCO1B3, 25 more genes
    nsv6927631copy number variation1nstd229human GRCh38 chr12: 21,638,470-21,641,951 , GRCh37.p13 chr12: 21,791,404-21,794,885 LDHB
    nsv6920316copy number variation1nstd229human GRCh38 chr12: 21,652,653-21,652,834 , GRCh37.p13 chr12: 21,805,587-21,805,768 LDHB
    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
    nsv6459058copy number variation1nstd223human GRCh38 chr12: 21,656,201-21,681,800 , GRCh37.p13 chr12: 21,809,135-21,834,734 LOC105369689, LDHB
    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
    nsv6313910copy number variation1nstd102humanUncertain significance GRCh37 chr12: 21,759,357-22,017,890 , GRCh38.p12 chr12: 21,606,423-21,864,956 KCNJ8, LOC102724261, 3 more genes
    nsv6309310copy number variation3nstd102humanUncertain significance GRCh37 chr12: 21,590,665-22,089,608 , GRCh38.p12 chr12: 21,437,731-21,936,674 LOC102724261, LDHB, 9 more genes
    nsv6202730copy number variation1nstd214human GRCh38 chr12: 21,648,910-21,648,992 , GRCh37.p13 chr12: 21,801,844-21,801,926 LDHB
    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
    nsv6132681copy number variation1nstd213human GRCh37 chr12: 21,770,000-21,990,001 , GRCh38.p12 chr12: 21,617,066-21,837,067 KCNJ8, LDHB, 3 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 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
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