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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
    nsv7147098insertion1nstd232human GRCh37.p13 chr2: 210,821,029-210,821,029 , GRCh38.p12 chr2: 209,956,305-209,956,305 UNC80
    nsv7138573insertion1nstd232human GRCh37.p13 chr2: 210,820,234-210,820,234 , GRCh38.p12 chr2: 209,955,510-209,955,510 UNC80
    nsv7096604copy number variation1nstd102humanPathogenic GRCh37 chr2: 210,636,797-213,403,254 , GRCh38.p12 chr2: 209,772,073-212,538,530 MTCO1P46, LOC100420775, 19 more genes
    nsv7096230copy number variation1nstd102humanUncertain significance GRCh37 chr2: 210,737,462-210,737,714 , GRCh38.p12 chr2: 209,872,738-209,872,990 UNC80
    nsv7096127copy number variation1nstd102humanUncertain significance GRCh37 chr2: 210,737,462-210,745,838 , GRCh38.p12 chr2: 209,872,738-209,881,114 UNC80
    nsv7046067inversion1nstd229human GRCh38 chr2: 209,787,325-209,798,320 , GRCh37.p13 chr2: 210,652,049-210,663,044 UNC80
    nsv6697516copy number variation1nstd229human GRCh38 chr2: 209,903,725-209,908,049 , GRCh37.p13 chr2: 210,768,449-210,772,773 UNC80
    nsv6697004copy number variation1nstd229human GRCh38 chr2: 209,977,401-209,981,900 , GRCh37.p13 chr2: 210,842,125-210,846,624 UNC80
    nsv6696131copy number variation1nstd229human GRCh38 chr2: 209,792,980-209,793,614 , GRCh37.p13 chr2: 210,657,704-210,658,338 UNC80
    nsv6695161copy number variation1nstd229human GRCh38 chr2: 209,863,101-209,867,500 , GRCh37.p13 chr2: 210,727,825-210,732,224 UNC80
    nsv6694216copy number variation1nstd229human GRCh38 chr2: 209,994,601-210,018,200 , GRCh37.p13 chr2: 210,859,325-210,882,924 UNC80, RPE
    nsv6693814copy number variation1nstd229human GRCh38 chr2: 209,745,022-209,880,959 , GRCh37.p13 chr2: 210,609,746-210,745,683 UNC80, SNAI1P1
    nsv6693780copy number variation1nstd229human GRCh38 chr2: 209,784,420-209,787,381 , GRCh37.p13 chr2: 210,649,144-210,652,105 UNC80
    nsv6691841copy number variation1nstd229human GRCh38 chr2: 209,853,492-209,865,017 , GRCh37.p13 chr2: 210,718,216-210,729,741 UNC80
    nsv6689586copy number variation1nstd229human GRCh38 chr2: 209,805,901-209,812,400 , GRCh37.p13 chr2: 210,670,625-210,677,124 SNAI1P1, UNC80
    nsv6689428copy number variation1nstd229human GRCh38 chr2: 209,882,001-209,886,700 , GRCh37.p13 chr2: 210,746,725-210,751,424 UNC80
    nsv6687798copy number variation1nstd229human GRCh38 chr2: 209,900,238-209,900,748 , GRCh37.p13 chr2: 210,764,962-210,765,472 UNC80
    nsv6687748copy number variation1nstd229human GRCh38 chr2: 209,910,189-209,918,128 , GRCh37.p13 chr2: 210,774,913-210,782,852 UNC80
    nsv6686587copy number variation1nstd229human GRCh38 chr2: 209,955,510-209,955,572 , GRCh37.p13 chr2: 210,820,234-210,820,296 UNC80
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