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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148155copy number variation1nstd102humanPathogenic GRCh37 chr17: 72,718,277-74,142,256 , GRCh38.p12 chr17: 74,722,138-76,146,175 TRIM65, TEN1, 74 more genes
    nsv7060867inversion1nstd229human GRCh38 chr17: 75,477,003-75,509,123 , GRCh37.p13 chr17: 73,473,084-73,505,204 TMEM94, CASKIN2, 1 more genes
    nsv6994443copy number variation1nstd229human GRCh38 chr17: 75,515,499-75,718,036 , GRCh37.p13 chr17: 73,511,580-73,714,116 CASKIN2, SAP30BP, 7 more genes
    nsv6991297copy number variation1nstd229human GRCh38 chr17: 75,491,201-75,503,200 , GRCh37.p13 chr17: 73,487,282-73,499,281 MIR6785, TMEM94, 1 more genes
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6983024copy number variation1nstd229human GRCh38 chr17: 75,494,709-75,505,079 , GRCh37.p13 chr17: 73,490,790-73,501,160 CASKIN2, TMEM94, 1 more genes
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6314018copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,049,227-73,533,226 , GRCh38.p12 chr17: 75,053,132-75,537,145 MIF4GD-DT, TSEN54, 21 more genes
    nsv6310407copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,204,602-73,515,148 , GRCh38.p12 chr17: 75,208,507-75,519,067 CASKIN2, MRPS7, 12 more genes
    nsv6133070copy number variation1nstd213human GRCh37 chr17: 62,460,000-73,800,001 , GRCh38.p12 chr17: 64,464,645-75,803,920 APOH, CACNG1, 225 more genes
    nsv5967778inversion1nstd209human GRCh37.p13 chr17: 73,502,206-73,606,416 , GRCh38 chr17: 75,506,125-75,610,335 , LLGL2, 3 more genes
    nsv5883861copy number variation1nstd209human GRCh38 chr17: 75,483,217-75,500,593 , GRCh37.p13 chr17: 73,479,298-73,496,674 CASKIN2, TMEM94, 1 more genes
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5016701copy number variation1nstd200human GRCh38 chr17: 75,497,331-75,501,634 , GRCh37.p13 chr17: 73,493,412-73,497,715 CASKIN2, TMEM94, 1 more genes
    nsv4854394copy number variation1nstd200human GRCh37 chr17: 73,511,580-73,714,116 , GRCh38.p12 chr17: 75,515,499-75,718,036 , CASKIN2, 8 more genes
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4628995copy number variation1nstd183human GRCh37 chr17: 73,217,773-73,774,243 , GRCh38.p12 chr17: 75,221,678-75,778,162 , LOC107985013, 23 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4457598copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,413,448-73,568,196 , GRCh38.p12 chr17: 75,417,367-75,572,115 MIR6785, LLGL2, 3 more genes
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