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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7057191inversion1nstd229human GRCh38 chr2: 219,392,741-219,619,982 , GRCh37.p13 chr2: 220,257,463-220,484,704 RN7SKP213, GMPPA, 13 more genes
    nsv7048316inversion1nstd229human GRCh38 chr2: 217,690,925-222,070,373 , GRCh37.p13 chr2: 218,555,648-222,935,092 LOC105373895, CXCR2P1, 119 more genes
    nsv7044013inversion1nstd229human GRCh38 chr2: 219,400,088-219,619,765 , GRCh37.p13 chr2: 220,264,810-220,484,487 TMEM198, RN7SKP213, 13 more genes
    nsv6693494copy number variation1nstd229human GRCh38 chr2: 219,542,463-219,564,177 , GRCh37.p13 chr2: 220,407,185-220,428,899 MIR3132, CHPF, 2 more genes
    nsv6683106copy number variation1nstd229human GRCh38 chr2: 219,541,785-219,552,173 , GRCh37.p13 chr2: 220,406,507-220,416,895 MIR3132, TMEM198, 2 more genes
    nsv6679518copy number variation1nstd229human GRCh38 chr2: 219,488,401-219,568,300 , GRCh37.p13 chr2: 220,353,123-220,433,022 SPEGNB, OBSL1, 7 more genes
    nsv6627822copy number variation1nstd224human GRCh37 chr2: 220,404,739-220,417,364 , GRCh38.p12 chr2: 219,540,017-219,552,642 TMEM198, OBSL1, 2 more genes
    nsv6627625copy number variation2nstd224human GRCh37 chr2: 220,404,739-220,419,340 , GRCh38.p12 chr2: 219,540,017-219,554,618 MIR3132, CHPF, 2 more genes
    nsv6346585copy number variation1nstd223human GRCh38 chr2: 219,120,801-219,643,000 , GRCh37.p13 chr2: 219,985,523-220,507,722 OBSL1, DNAJB2, 32 more genes
    nsv6343381copy number variation1nstd223human GRCh38 chr2: 219,100,201-219,804,900 , GRCh37.p13 chr2: 219,964,923-220,669,621 CHPF, TMEM198, 38 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313686copy number variation1nstd102humanPathogenic GRCh37 chr2: 215,108,009-221,679,980 , GRCh38.p12 chr2: 214,243,285-220,815,260 BCS1L, LOC105373880, 160 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 LOC105373947, RN7SL764P, 357 more genes
    nsv6311374copy number variation2nstd102humanUncertain significance GRCh37 chr2: 218,999,525-220,435,954 , GRCh38.p12 chr2: 218,134,802-219,571,232 CHPF, WNT6, 83 more genes
    nsv6134651copy number variation1nstd213human GRCh37 chr2: 220,280,000-220,570,001 , GRCh38.p12 chr2: 219,415,278-219,705,279 DES, INHA, 14 more genes
    nsv6112757copy number variation1nstd102humanPathogenic GRCh37 chr2: 220,056,891-227,164,817 , GRCh38.p12 chr2: 219,192,169-226,300,101 DES, SPEG, 100 more genes
    nsv5987649copy number variation1nstd212human GRCh38 chr2: 219,541,965-219,542,206 , GRCh37.p13 chr2: 220,406,687-220,406,928 CHPF, TMEM198
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
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