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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099193copy number variation1nstd231human GRCh38.p12 chr1: 32,456,017-38,905,781 , GRCh37 chr1: 32,921,618-39,371,453 AK2, COL8A2, 151 more genes
    nsv7054580inversion1nstd229human GRCh38 chr1: 33,076,956-33,688,708 , GRCh37.p13 chr1: 33,542,557-34,154,308 RN7SKP16, ZNF362, 11 more genes
    nsv7046389inversion1nstd229human GRCh38 chr1: 31,492,639-36,569,102 , GRCh37.p13 chr1: 32,017,064-37,034,703 LOC105378642, TMEM35B, 127 more genes
    nsv6649151copy number variation1nstd229human GRCh38 chr1: 33,183,923-33,187,273 , GRCh37.p13 chr1: 33,649,524-33,652,874 TRIM62
    nsv6649150copy number variation1nstd229human GRCh38 chr1: 33,175,699-33,175,781 , GRCh37.p13 chr1: 33,641,300-33,641,382 TRIM62
    nsv6649149copy number variation1nstd229human GRCh38 chr1: 33,147,955-33,150,864 , GRCh37.p13 chr1: 33,613,556-33,616,465 AZIN2, TRIM62
    nsv6649002copy number variation1nstd229human GRCh38 chr1: 33,170,101-33,174,000 , GRCh37.p13 chr1: 33,635,702-33,639,601 TRIM62
    nsv6648959copy number variation1nstd229human GRCh38 chr1: 33,174,903-33,174,963 , GRCh37.p13 chr1: 33,640,504-33,640,564 TRIM62
    nsv6648957copy number variation1nstd229human GRCh38 chr1: 33,152,466-33,154,698 , GRCh37.p13 chr1: 33,618,067-33,620,299 TRIM62, AZIN2
    nsv6648920copy number variation1nstd229human GRCh38 chr1: 33,034,541-33,209,380 , GRCh37.p13 chr1: 33,500,142-33,674,981 TRIM62, AZIN2, 2 more genes
    nsv6648500copy number variation1nstd229human GRCh38 chr1: 33,170,465-33,174,035 , GRCh37.p13 chr1: 33,636,066-33,639,636 TRIM62
    nsv6648499copy number variation1nstd229human GRCh38 chr1: 33,150,323-33,150,651 , GRCh37.p13 chr1: 33,615,924-33,616,252 AZIN2, TRIM62
    nsv6335506copy number variation1nstd223human GRCh38 chr1: 33,183,923-33,187,272 , GRCh37.p13 chr1: 33,649,524-33,652,873 TRIM62
    nsv6330549copy number variation1nstd223human GRCh38 chr1: 33,165,946-33,167,137 , GRCh37.p13 chr1: 33,631,547-33,632,738 TRIM62
    nsv6319707copy number variation1nstd223human GRCh38 chr1: 33,170,453-33,174,034 , GRCh37.p13 chr1: 33,636,054-33,639,635 TRIM62
    nsv6319577copy number variation1nstd223human GRCh38 chr1: 33,184,970-33,191,694 , GRCh37.p13 chr1: 33,650,571-33,657,295 TRIM62
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
    nsv6299105copy number variation1nstd186human GRCh37 chr1: 33,614,448-33,616,588 , GRCh38.p12 chr1: 33,148,847-33,150,987 TRIM62, AZIN2
    nsv6219222insertion1nstd214human GRCh38 chr1: 33,180,818-33,180,818 , GRCh37.p13 chr1: 33,646,419-33,646,419 TRIM62
    nsv6166154copy number variation1nstd214human GRCh38 chr1: 33,175,702-33,175,780 , GRCh37.p13 chr1: 33,641,303-33,641,381 TRIM62
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