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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
    nsv7096242copy number variation1nstd102humanPathogenic GRCh37 chr2: 220,434,923-220,435,954 , GRCh38.p12 chr2: 219,570,201-219,571,232 INHA, OBSL1
    nsv7096241copy number variation1nstd102humanUncertain significance GRCh37 chr2: 220,427,104-220,435,954 , GRCh38.p12 chr2: 219,562,382-219,571,232 INHA, OBSL1
    nsv7096138copy number variation1nstd102humanPathogenic GRCh37 chr2: 220,415,557-220,435,954 , GRCh38.p12 chr2: 219,550,835-219,571,232 TMEM198, OBSL1, 1 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
    nsv6685249copy number variation1nstd229human GRCh38 chr2: 219,561,347-219,571,478 , GRCh37.p13 chr2: 220,426,069-220,436,200 INHA, OBSL1
    nsv6679437copy number variation1nstd229human GRCh38 chr2: 219,574,697-219,621,916 , GRCh37.p13 chr2: 220,439,419-220,486,638 INHA, STK11IP, 1 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
    nsv6342297copy number variation1nstd223human GRCh38 chr2: 219,561,347-219,571,478 , GRCh37.p13 chr2: 220,426,069-220,436,200 OBSL1, INHA
    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
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5361337translocation1nstd200human GRCh38 chr2: 219,574,412-219,574,412 , GRCh38 chr2: 219,572,007-219,572,007 , GRCh37.p13 chr2: 220,439,134-220,439,134 , GRCh37.p13 chr2: 220,436,729-220,436,729 OBSL1, INHA
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