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Items: 1 to 20 of 352

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137687insertion1nstd232human GRCh37.p13 chr2: 27,074,203-27,074,203 , GRCh38.p12 chr2: 26,851,335-26,851,335 DPYSL5
    nsv7096625copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,443,763-30,143,525 , GRCh38.p12 chr2: 24,220,894-29,920,659 LOC105374381, POMC, 136 more genes
    nsv7096148copy number variation2nstd102humanUncertain significance GRCh37 chr2: 24,443,763-29,022,169 , GRCh38.p12 chr2: 24,220,894-28,799,303 LOC105374381, SLC35F6, 122 more genes
    nsv7042984inversion1nstd229human GRCh38 chr2: 26,886,657-32,818,427 , GRCh37.p13 chr2: 27,109,525-33,043,494 CLIP4, LOC102723594, 118 more genes
    nsv7042712inversion1nstd229human GRCh38 chr2: 26,895,322-26,908,934 , GRCh37.p13 chr2: 27,118,190-27,131,802 DPYSL5
    nsv7038143inversion1nstd229human GRCh38 chr2: 26,920,140-26,932,337 , GRCh37.p13 chr2: 27,143,008-27,155,205 DPYSL5
    nsv6677017copy number variation1nstd229human GRCh38 chr2: 26,933,434-26,934,057 , GRCh37.p13 chr2: 27,156,302-27,156,925 DPYSL5
    nsv6676401copy number variation1nstd229human GRCh38 chr2: 26,811,477-26,847,274 , GRCh37.p13 chr2: 27,034,345-27,070,142 CDKN2AIPNLP2, DPYSL5
    nsv6672785copy number variation1nstd229human GRCh38 chr2: 24,384,939-32,866,867 , GRCh37.p13 chr2: 24,607,808-33,091,934 CENPO, TOGARAM2, 170 more genes
    nsv6668226copy number variation1nstd229human GRCh38 chr2: 26,850,001-26,892,300 , GRCh37.p13 chr2: 27,072,869-27,115,168 DPYSL5
    nsv6667418copy number variation1nstd229human GRCh38 chr2: 26,758,538-26,901,747 , GRCh37.p13 chr2: 26,981,406-27,124,615 CDKN2AIPNLP2, CENPA, 2 more genes
    nsv6667045copy number variation1nstd229human GRCh38 chr2: 26,856,801-26,860,700 , GRCh37.p13 chr2: 27,079,669-27,083,568 DPYSL5
    nsv6666888copy number variation1nstd229human GRCh38 chr2: 26,887,694-26,887,755 , GRCh37.p13 chr2: 27,110,562-27,110,623 DPYSL5
    nsv6665320copy number variation1nstd229human GRCh38 chr2: 26,904,401-26,909,500 , GRCh37.p13 chr2: 27,127,269-27,132,368 DPYSL5
    nsv6664466copy number variation1nstd229human GRCh38 chr2: 26,885,245-26,891,659 , GRCh37.p13 chr2: 27,108,113-27,114,527 DPYSL5
    nsv6663318copy number variation1nstd229human GRCh38 chr2: 26,867,701-26,888,500 , GRCh37.p13 chr2: 27,090,569-27,111,368 DPYSL5
    nsv6661382copy number variation1nstd229human GRCh38 chr2: 26,930,171-26,930,627 , GRCh37.p13 chr2: 27,153,039-27,153,495 DPYSL5
    nsv6659021copy number variation1nstd229human GRCh38 chr2: 26,885,301-26,891,600 , GRCh37.p13 chr2: 27,108,169-27,114,468 DPYSL5
    nsv6658658copy number variation1nstd229human GRCh38 chr2: 26,867,880-26,880,758 , GRCh37.p13 chr2: 27,090,748-27,103,626 DPYSL5
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
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