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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974534inversion1nstd209human GRCh38 chr17: 15,750,079-18,634,890 , GRCh37.p13 chr17: 15,653,393-18,538,203 , ADORA2B, 119 more genes
    nsv5933579copy number variation1nstd209human GRCh38 chr17: 16,936,959-20,558,118 , GRCh37.p13 chr17: 16,840,273-20,461,431 , FAM106B, 146 more genes
    nsv5713107mobile element insertion1nstd211human GRCh38 chr17: 17,775,026-17,775,026 , GRCh37.p13 chr17: 17,678,340-17,678,340 RAI1, SMCR5
    nsv5665112inversion1nstd207human GRCh37.p13 chr17: 16,704,599-18,417,421 , GRCh38 chr17: 16,801,285-18,514,107 , DRG2, 71 more genes
    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
    nsv5381795copy number variation1nstd102humanUncertain significance GRCh37 chr17: 17,104,302-17,690,077 , GRCh38.p12 chr17: 17,200,988-17,786,763 RPL13P12, ACTG1P24, 15 more genes
    nsv5280936copy number variation1nstd204human GRCh38.p13 chr17: 17,763,701-18,133,000 , GRCh37.p13 chr17: 17,667,015-18,036,314 GID4, MIR33B, 14 more genes
    nsv5155412mobile element insertion1nstd203human GRCh38 chr17: 17,775,009-17,775,024 , GRCh37.p13 chr17: 17,678,323-17,678,338 RAI1, SMCR5
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 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
    nsv4729796copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 17,614,338-17,911,166 , GRCh38.p12 chr17: 17,711,024-18,007,852 SREBF1, RAI1, 8 more genes
    nsv4729738copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,810,015-18,537,436 , GRCh38.p12 chr17: 15,906,701-18,634,123 UPF3AP1, ADORA2B, 109 more genes
    nsv4675003copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,632,431-18,726,389 , GRCh38.p12 chr17: 15,729,117-18,823,076 LLGL1, LOC107985051, 127 more genes
    nsv4513863mobile element insertion1nstd166human GRCh37.p13 chr17: 17,678,323-17,678,323 , GRCh38.p12 chr17: 17,775,009-17,775,009 RAI1, SMCR5
    nsv4457849copy number variation1nstd102humanUncertain significance GRCh37 chr17: 17,615,338-17,743,219 , GRCh38.p12 chr17: 17,712,024-17,839,905 RAI1, MIR33B, 4 more genes
    nsv4436751copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,908,991-18,322,254 , GRCh38.p12 chr17: 17,005,677-18,418,940 RPL7AP65, TOP3A, 46 more genes
    nsv4349342copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,842,991-20,217,316 , GRCh38.p12 chr17: 16,939,677-20,314,003 LOC105371566, LOC105371569, 126 more genes
    nsv4249733copy number variation1nstd166human GRCh37.p13 chr17: 17,681,960-17,682,013 , GRCh38.p12 chr17: 17,778,646-17,778,699 RAI1, SMCR5
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