U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 129

    loading data ...

    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
    nsv6697800copy number variation1nstd229human GRCh38 chr2: 219,495,631-219,513,654 , GRCh37.p13 chr2: 220,360,353-220,378,376 GMPPA, SPEGNB, 2 more genes
    nsv6696346copy number variation1nstd229human GRCh38 chr2: 219,477,827-219,508,228 , GRCh37.p13 chr2: 220,342,549-220,372,950 SPEG, SPEGNB, 2 more genes
    nsv6695207copy number variation1nstd229human GRCh38 chr2: 219,503,878-219,510,020 , GRCh37.p13 chr2: 220,368,600-220,374,742 GMPPA, ASIC4-AS1
    nsv6685288copy number variation1nstd229human GRCh38 chr2: 219,439,108-219,510,653 , GRCh37.p13 chr2: 220,303,830-220,375,375 ASIC4-AS1, SPEG, 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
    nsv6351774copy number variation1nstd223human GRCh38 chr2: 219,496,063-219,497,550 , GRCh37.p13 chr2: 220,360,785-220,362,272 GMPPA, SPEGNB, 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
    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
    nsv5361335translocation1nstd200human GRCh38 chr2: 219,496,063-219,496,063 , GRCh38 chr2: 219,497,550-219,497,550 , GRCh37.p13 chr2: 220,362,272-220,362,272 , GRCh37.p13 chr2: 220,360,785-220,360,785 GMPPA, SPEGNB, 1 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center