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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
    nsv5972005insertion1nstd209human GRCh38 chr17: 19,694,977-19,694,977 , GRCh37.p13 chr17: 19,598,290-19,598,290 SLC47A2
    nsv5933579copy number variation1nstd209human GRCh38 chr17: 16,936,959-20,558,118 , GRCh37.p13 chr17: 16,840,273-20,461,431 , FAM106B, 146 more genes
    nsv5713525mobile element insertion2nstd211human GRCh38 chr17: 19,694,993-19,694,993 , GRCh37.p13 chr17: 19,598,306-19,598,306 SLC47A2
    nsv5670902inversion1nstd207human GRCh37.p13 chr17: 19,143,942-21,250,947 , GRCh38 chr17: 19,240,629-21,558,840 , ALDH3A1, 86 more genes
    nsv5651719insertion1nstd207human GRCh38 chr17: 19,694,977-19,694,977 , GRCh37.p13 chr17: 19,598,290-19,598,290 SLC47A2
    nsv5532656copy number variation1nstd206human GRCh38 chr17: 19,673,743-19,679,323 , GRCh37.p13 chr17: 19,577,056-19,582,636 ALDH3A2, SLC47A2
    nsv5526851copy number variation1nstd206human GRCh38 chr17: 19,717,335-19,717,843 , GRCh37.p13 chr17: 19,620,648-19,621,156 SLC47A2
    nsv5429497mobile element insertion1nstd206human GRCh38 chr17: 19,694,993-19,695,044 , GRCh37.p13 chr17: 19,598,306-19,598,357 SLC47A2
    nsv5381800copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,601,603-20,063,369 , GRCh38.p12 chr17: 16,698,289-20,160,056 COTL1P1, LOC105371551, 141 more genes
    nsv5381797copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,145,361-20,137,943 , GRCh38.p12 chr17: 17,242,047-20,234,630 LOC644909, FLII, 117 more genes
    nsv5155709mobile element insertion1nstd203human GRCh38 chr17: 19,694,977-19,694,993 , GRCh37.p13 chr17: 19,598,290-19,598,306 SLC47A2
    nsv5026207copy number variation1nstd200human GRCh38 chr17: 19,717,335-19,717,843 , GRCh37.p13 chr17: 19,620,648-19,621,156 SLC47A2
    nsv5026206copy number variation1nstd200human GRCh38 chr17: 19,679,676-19,714,831 , GRCh37.p13 chr17: 19,582,989-19,618,144 SLC47A2
    nsv4858313copy number variation1nstd200human GRCh37 chr17: 19,582,989-19,618,144 , GRCh38.p12 chr17: 19,679,676-19,714,831 SLC47A2
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729895copy number variation1nstd102humanUncertain significance GRCh37 chr17: 18,746,987-20,231,379 , GRCh38.p12 chr17: 18,843,674-20,328,066 NDUFB4P3, SNORD3A, 52 more genes
    nsv4729886copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,763,370-20,395,611 , GRCh38.p12 chr17: 16,860,056-20,492,298 LOC100419620, PAIP1P2, 139 more genes
    nsv4729810copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,761,814-20,330,062 , GRCh38.p12 chr17: 16,858,500-20,426,749 PRPSAP2, EPN2, 134 more genes
    nsv4675696copy number variation1nstd102humanUncertain significance GRCh37 chr17: 19,356,083-19,917,814 , GRCh38.p12 chr17: 19,452,770-20,014,501 SLC47A2, TRW-CCA2-1, 18 more genes
    nsv4675203copy number variation1nstd102humanUncertain significance GRCh37 chr17: 19,574,666-19,624,308 , GRCh38.p12 chr17: 19,671,353-19,720,995 SLC47A2, ALDH3A2
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