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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
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7094209copy number variation2nstd102humanUncertain significance GRCh37 chr12: 21,918,657-22,017,431 , GRCh38.p12 chr12: 21,765,723-21,864,497 ABCC9, LOC105369689, 1 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
    nsv7065912inversion1nstd229human GRCh38 chr12: 21,665,209-21,782,445 , GRCh37.p13 chr12: 21,818,143-21,935,379 KCNJ8, LOC102724261, 1 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
    nsv7059147inversion1nstd229human GRCh38 chr12: 21,659,104-21,765,310 , GRCh37.p13 chr12: 21,812,038-21,918,244 LOC102724261, KCNJ8, 1 more genes
    nsv6926517copy number variation1nstd229human GRCh38 chr12: 21,775,901-21,798,300 , GRCh37.p13 chr12: 21,928,835-21,951,234 LOC105369689, ABCC9, 1 more genes
    nsv6921182copy number variation1nstd229human GRCh38 chr12: 21,765,301-21,782,500 , GRCh37.p13 chr12: 21,918,235-21,935,434 LOC105369689, KCNJ8
    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
    nsv6591644inversion1nstd223human GRCh38 chr12: 21,692,689-21,866,315 , GRCh37.p13 chr12: 21,845,623-22,019,249 KCNJ8, ABCC9, 2 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
    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
    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
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