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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
    nsv7064789inversion1nstd229human GRCh38 chr12: 10,249,571-12,880,432 , GRCh37.p13 chr12: 10,402,170-13,033,366 DDX47, TAS2R64P, 89 more genes
    nsv7064629inversion1nstd229human GRCh38 chr12: 10,296,462-11,054,955 , GRCh37.p13 chr12: 10,449,061-11,207,554 TAS2R31, EIF2S3B, 39 more genes
    nsv7063770inversion1nstd229human GRCh38 chr12: 10,733,366-10,733,412 , GRCh37.p13 chr12: 10,885,965-10,886,011 LOC112268104
    nsv7061545inversion1nstd229human GRCh38 chr12: 10,483,551-11,289,523 , GRCh37.p13 chr12: 10,636,150-11,442,457 TAS2R14, EIF2S3B, 40 more genes
    nsv6931101copy number variation1nstd229human GRCh38 chr12: 10,720,422-10,881,002 , GRCh37.p13 chr12: 10,873,021-11,033,601 PRR4, HSPE1P12, 10 more genes
    nsv6929493copy number variation1nstd229human GRCh38 chr12: 10,724,901-10,733,700 , GRCh37.p13 chr12: 10,877,500-10,886,299 LOC112268104
    nsv6919587copy number variation1nstd229human GRCh38 chr12: 10,732,555-10,742,492 , GRCh37.p13 chr12: 10,885,154-10,895,091 LOC112268104
    nsv6918322copy number variation1nstd229human GRCh38 chr12: 10,729,701-10,732,400 , GRCh37.p13 chr12: 10,882,300-10,884,999 LOC112268104
    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
    nsv6465372copy number variation1nstd223human GRCh38 chr12: 10,720,422-10,881,002 , GRCh37.p13 chr12: 10,873,021-11,033,601 PRR4, HSPE1P12, 10 more genes
    nsv6307883insertion1nstd186human GRCh37 chr12: 10,879,877-10,879,913 , GRCh38.p12 chr12: 10,727,278-10,727,314 LOC112268104
    nsv6274253copy number variation1nstd214human GRCh38 chr12: 10,739,707-10,739,773 , GRCh37.p13 chr12: 10,892,306-10,892,372 LOC112268104
    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
    nsv6132445copy number variation1nstd213human GRCh37 chr12: 9,040,000-11,190,001 , GRCh38.p12 chr12: 8,887,404-11,037,402 A2M, A2MP1, 95 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
    nsv6132133copy number variation1nstd213human GRCh37 chr12: 10,400,000-11,220,001 , GRCh38.p12 chr12: 10,247,401-11,067,402 KLRC2, PRH1, 41 more genes
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