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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074310inversion1nstd229human GRCh38 chr14: 22,076,285-27,854,954 , GRCh37.p13 chr14: 22,544,546-28,324,160 PPP1R3E, TRAJ37, 242 more genes
    nsv7064877inversion1nstd229human GRCh38 chr14: 27,224,536-29,285,975 , GRCh37.p13 chr14: 27,693,742-29,755,181 LINC02326, LINC02300, 19 more genes
    nsv7063677inversion1nstd229human GRCh38 chr14: 25,538,587-28,937,476 , GRCh37.p13 chr14: 26,007,793-29,406,682 MIR3171HG, LINC02327, 28 more genes
    nsv7063304inversion1nstd229human GRCh38 chr14: 25,686,195-28,154,468 , GRCh37.p13 chr14: 26,155,401-28,623,674 LOC105370418, LINC02294, 15 more genes
    nsv6955523copy number variation1nstd229human GRCh38 chr14: 27,615,326-27,668,755 , GRCh37.p13 chr14: 28,084,532-28,137,961 MIR3171HG, MIR3171, 1 more genes
    nsv6951366copy number variation1nstd229human GRCh38 chr14: 27,560,011-27,669,536 , GRCh37.p13 chr14: 28,029,217-28,138,742 LINC00645, MIR3171, 1 more genes
    nsv6949819copy number variation1nstd229human GRCh38 chr14: 27,513,961-27,647,939 , GRCh37.p13 chr14: 27,983,167-28,117,145 MIR3171, LINC00645, 1 more genes
    nsv6947547copy number variation1nstd229human GRCh38 chr14: 27,558,678-27,673,455 , GRCh37.p13 chr14: 28,027,884-28,142,661 MIR3171HG, MIR3171, 1 more genes
    nsv6947467copy number variation1nstd229human GRCh38 chr14: 27,466,132-27,726,342 , GRCh37.p13 chr14: 27,935,338-28,195,548 LINC00645, MIR3171, 1 more genes
    nsv6947031copy number variation1nstd229human GRCh38 chr14: 27,639,101-27,798,300 , GRCh37.p13 chr14: 28,108,307-28,267,506 LINC00645, MIR3171HG
    nsv6946383copy number variation1nstd229human GRCh38 chr14: 27,333,932-28,640,200 , GRCh37.p13 chr14: 27,803,138-29,109,406 LINC02300, RPL26P3, 6 more genes
    nsv6945872copy number variation1nstd229human GRCh38 chr14: 27,412,039-27,612,679 , GRCh37.p13 chr14: 27,881,245-28,081,885 LINC00645, MIR3171HG
    nsv6945622copy number variation1nstd229human GRCh38 chr14: 27,627,538-27,639,862 , GRCh37.p13 chr14: 28,096,744-28,109,068 LINC00645, MIR3171, 1 more genes
    nsv6945413copy number variation1nstd229human GRCh38 chr14: 27,367,901-27,612,000 , GRCh37.p13 chr14: 27,837,107-28,081,206 LINC00645, MIR3171HG
    nsv6944315copy number variation1nstd229human GRCh38 chr14: 27,622,519-27,760,275 , GRCh37.p13 chr14: 28,091,725-28,229,481 MIR3171HG, MIR3171, 1 more genes
    nsv6943342copy number variation1nstd229human GRCh38 chr14: 27,026,319-27,750,762 , GRCh37.p13 chr14: 27,495,525-28,219,968 LOC105370420, LOC105370421, 4 more genes
    nsv6942489copy number variation1nstd229human GRCh38 chr14: 27,548,726-27,628,278 , GRCh37.p13 chr14: 28,017,932-28,097,484 LINC00645, MIR3171HG
    nsv6940879copy number variation1nstd229human GRCh38 chr14: 27,501,865-27,767,884 , GRCh37.p13 chr14: 27,971,071-28,237,090 MIR3171, LINC00645, 1 more genes
    nsv6940039copy number variation1nstd229human GRCh38 chr14: 27,548,062-27,627,773 , GRCh37.p13 chr14: 28,017,268-28,096,979 MIR3171HG, LINC00645
    nsv6637416copy number variation1nstd102humanPathogenic GRCh37 chr14: 24,959,823-33,415,359 , GRCh38.p12 chr14: 24,490,617-32,946,153 SCFD1, RPL12P5, 94 more genes
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