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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142331insertion1nstd232human GRCh37.p13 chr1: 150,939,963-150,939,963 , GRCh38.p12 chr1: 150,967,487-150,967,487 CERS2
    nsv7099231copy number variation1nstd231human GRCh38.p12 chr1: 149,962,894-151,006,586 , GRCh37 chr1: 149,934,818-150,979,062 ARNT, CTSK, 48 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
    nsv6641777copy number variation1nstd229human GRCh38 chr1: 150,967,801-151,307,200 , GRCh37.p13 chr1: 150,940,277-151,279,676 MINDY1, TNFAIP8L2, 23 more genes
    nsv6641764copy number variation1nstd229human GRCh38 chr1: 150,761,787-151,277,656 , GRCh37.p13 chr1: 150,734,263-151,250,132 VPS72, RPS29P29, 30 more genes
    nsv6330594copy number variation1nstd223human GRCh38 chr1: 150,969,402-150,980,223 , GRCh37.p13 chr1: 150,941,878-150,952,699 CERS2, LOC105371438
    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
    nsv6133734copy number variation1nstd213human GRCh37 chr1: 150,350,000-154,440,001 , GRCh38.p12 chr1: 150,377,524-154,467,525 , MCL1, 216 more genes
    nsv6133733copy number variation1nstd213human GRCh37 chr1: 149,980,000-151,620,001 , GRCh38.p12 chr1: 150,008,051-151,647,525 CTSK, MCL1, 80 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
    nsv6133499copy number variation1nstd213human GRCh37 chr1: 149,880,000-153,720,001 , GRCh38.p12 chr1: 149,908,448-153,747,525 , CTSK, 198 more genes
    nsv5415627copy number variation1nstd206human GRCh38 chr1: 150,969,152-150,969,223 , GRCh37.p13 chr1: 150,941,628-150,941,699 CERS2
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4728712copy number variation1nstd102humanUncertain significance GRCh37 chr1: 150,611,086-150,941,270 , GRCh38.p12 chr1: 150,638,610-150,968,794 RNU6-1309P, RPS27AP6, 13 more genes
    nsv4705049copy number variation1nstd195human GRCh37 chr1: 150,824,351-151,042,101 , GRCh38.p12 chr1: 150,851,875-151,069,625 ARNT, ANXA9, 15 more genes
    nsv4579565copy number variation1nstd183human GRCh37 chr1: 150,940,296-150,940,472 , GRCh38.p12 chr1: 150,967,820-150,967,996 CERS2
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