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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7145288copy number variation1nstd232human GRCh37.p13 chr17: 957,935-957,984 , GRCh38.p12 chr17: 1,054,695-1,054,744 , GRCh38.p12 chr17|NT_187664.1: 93,084-93,133 , GRCh38.p12 chr17|NT_187613.1: 93,236-93,285 ABR
    nsv7145053copy number variation1nstd232human GRCh37.p13 chr17: 957,860-957,909 , GRCh38.p12 chr17: 1,054,620-1,054,669 ABR
    nsv7144863copy number variation1nstd232human GRCh37.p13 chr17: 940,271-940,329 , GRCh38.p12 chr17: 1,037,031-1,037,089 , GRCh38.p12 chr17|NT_187664.1: 76,278-76,336 , GRCh38.p12 chr17|NT_187613.1: 76,278-76,336 ABR
    nsv7144586copy number variation1nstd232human GRCh37.p13 chr17: 938,642-938,702 , GRCh38.p12 chr17: 1,035,402-1,035,462 , GRCh38.p12 chr17|NT_187664.1: 74,649-74,709 , GRCh38.p12 chr17|NT_187613.1: 74,649-74,709 ABR
    nsv7143903copy number variation1nstd232human GRCh37.p13 chr17: 933,020-933,078 , GRCh38.p12 chr17: 1,029,780-1,029,838 , GRCh38.p12 chr17|NT_187664.1: 69,027-69,085 , GRCh38.p12 chr17|NT_187613.1: 69,027-69,085 ABR
    nsv7142015insertion1nstd232human GRCh37.p13 chr17: 933,167-933,167 , GRCh38.p12 chr17: 1,029,927-1,029,927 , GRCh38.p12 chr17|NT_187664.1: 69,174-69,174 , GRCh38.p12 chr17|NT_187613.1: 69,174-69,174 ABR
    nsv7138257copy number variation1nstd232human GRCh37.p13 chr17: 967,333-967,415 , GRCh38.p12 chr17|NT_187613.1: 107,375-107,460 , GRCh38.p12 chr17: 1,064,093-1,064,175 ABR
    nsv7098743copy number variation1nstd102humanUncertain significance GRCh37 chr17: 422,368-2,585,096 , GRCh38.p12 chr17: 519,128-2,681,802 PAFAH1B1, RN7SL33P, 65 more genes
    nsv7098729copy number variation1nstd102humanPathogenic GRCh37 chr17: 422,368-1,945,151 , GRCh38.p12 chr17: 519,128-2,041,857 MYO1C, SERPINF1, 42 more genes
    nsv7094928copy number variation1nstd102humanPathogenic GRCh37 chr17: 882,539-1,387,567 , GRCh38.p12 chr17: 979,299-1,484,273 , GRCh38.p12 chr17|NT_187613.1: 18,546-391,357 MIR3183, ABR, 11 more genes
    nsv7094896copy number variation1nstd102humanUncertain significance GRCh37 chr17: 422,368-1,680,740 , GRCh38.p12 chr17: 519,128-1,777,446 SLC43A2, LOC105371480, 34 more genes
    nsv7077625inversion1nstd229human GRCh38 chr17: 626,377-3,112,687 , GRCh37.p13 chr17: 529,617-3,015,981 MIR3183, YWHAE, 75 more genes
    nsv7075236inversion1nstd229human GRCh38 chr17: 1,196,205-1,199,639 , GRCh37.p13 chr17: 1,099,499-1,102,933 ABR
    nsv7073912inversion1nstd229human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 TNFSF12, SCARNA21, 321 more genes
    nsv7073434inversion1nstd229human GRCh38 chr17: 1,134,974-1,270,137 , GRCh37.p13 chr17: 1,038,189-1,173,431 LOC105371480, ABR-AS1, 3 more genes
    nsv7072236inversion1nstd229human GRCh38 chr17: 1,201,901-1,240,741 , GRCh37.p13 chr17: 1,105,195-1,144,035 ABR
    nsv7071122inversion1nstd229human GRCh38 chr17: 998,869-1,017,097 , GRCh37.p13 chr17: 902,109-920,337 LOC105371481, ABR, 1 more genes
    nsv7067543inversion1nstd229human GRCh38 chr17: 1,101,622-1,101,692 , GRCh37.p13 chr17: 1,004,862-1,004,932 ABR
    nsv7065520inversion1nstd229human GRCh38 chr17: 1,132,143-1,236,236 , GRCh37.p13 chr17: 1,035,361-1,139,530 ABR-AS1, ABR, 2 more genes
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