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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099232copy number variation1nstd231human GRCh38.p12 chr1: 151,364,317-152,231,192 , GRCh37 chr1: 151,336,793-152,203,668 , PSMB4, 37 more genes
    nsv7056666inversion1nstd229human GRCh38 chr1: 151,403,323-155,722,147 , GRCh37.p13 chr1: 151,375,799-155,691,938 ILF2, SPRR2C, 219 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7044458inversion1nstd229human GRCh38 chr1: 150,355,899-155,246,175 , GRCh37.p13 chr1: 150,440,214-155,215,966 LCE2C, MUC1, 254 more genes
    nsv7042502inversion1nstd229human GRCh38 chr1: 150,301,267-155,517,761 , GRCh37.p13 chr1: 150,440,214-155,487,552 LINGO4, CELF3, 268 more genes
    nsv6642170copy number variation1nstd229human GRCh38 chr1: 151,594,401-152,005,700 , GRCh37.p13 chr1: 151,566,877-151,978,176 CELF3, LINGO4, 17 more genes
    nsv6642026copy number variation1nstd229human GRCh38 chr1: 151,766,988-151,797,820 , GRCh37.p13 chr1: 151,739,464-151,770,296 TDRKH-AS1, TDRKH, 2 more genes
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6224686insertion2nstd214human GRCh38 chr1: 151,769,286-151,769,286 , GRCh37.p13 chr1: 151,741,762-151,741,762 TDRKH, OAZ3
    nsv6212633insertion2nstd214human GRCh38 chr1: 151,769,293-151,769,293 , GRCh37.p13 chr1: 151,741,769-151,741,769 OAZ3, TDRKH
    nsv6133734copy number variation1nstd213human GRCh37 chr1: 150,350,000-154,440,001 , GRCh38.p12 chr1: 150,377,524-154,467,525 , MCL1, 216 more genes
    nsv6133732copy number variation1nstd213human GRCh37 chr1: 149,750,000-153,310,001 , GRCh38.p12 chr1: 149,778,444-153,337,525 , CTSK, 183 more genes
    nsv6133555copy number variation1nstd213human GRCh37 chr1: 151,620,000-151,990,001 , GRCh38.p12 chr1: 151,647,524-152,017,525 RORC, THEM4, 18 more genes
    nsv6133499copy number variation1nstd213human GRCh37 chr1: 149,880,000-153,720,001 , GRCh38.p12 chr1: 149,908,448-153,747,525 , CTSK, 198 more genes
    nsv6126162insertion1nstd186human GRCh37 chr1: 151,741,762-151,741,762 , GRCh38.p12 chr1: 151,769,286-151,769,286 OAZ3, TDRKH
    nsv6053980insertion1nstd212human GRCh38 chr1: 151,771,806-151,771,806 , GRCh37.p13 chr1: 151,744,282-151,744,282 OAZ3, TDRKH
    nsv6044377insertion1nstd212human GRCh38 chr1: 151,769,293-151,769,293 , GRCh37.p13 chr1: 151,741,769-151,741,769 TDRKH, OAZ3
    nsv5964724insertion1nstd209human GRCh38 chr1: 151,769,286-151,769,286 , GRCh37.p13 chr1: 151,741,762-151,741,762 TDRKH, OAZ3
    nsv5878582copy number variation1nstd209human GRCh38 chr1: 151,762,500-151,762,988 , GRCh37.p13 chr1: 151,734,976-151,735,464 OAZ3, MRPL9
    nsv5877299copy number variation1nstd209human GRCh38 chr1: 151,760,899-151,761,449 , GRCh37.p13 chr1: 151,733,375-151,733,925 OAZ3, MRPL9
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