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Items: 1 to 20 of 254

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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
    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
    nsv5026095copy number variation1nstd200human GRCh38 chr17: 17,168,826-17,168,931 , GRCh37.p13 chr17: 17,072,140-17,072,245 MPRIP, RNU6-767P
    nsv4858230copy number variation1nstd200human GRCh37 chr17: 17,072,140-17,072,245 , GRCh38.p12 chr17: 17,168,826-17,168,931 RNU6-767P, MPRIP
    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
    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
    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
    nsv4323776inversion1nstd166human GRCh37.p13 chr17: 12,686,463-17,083,896 , GRCh38.p12 chr17: 12,783,146-17,180,582 , IL6STP1, 104 more genes
    nsv3959264inversion1nstd168human GRCh38 chr17: 16,699,407-18,631,342 , GRCh37.p13 chr17: 16,602,721-18,534,655 , DRG2, 81 more genes
    nsv3924768copy number variation1nstd102humanPathogenic GRCh38 chr17: 16,713,514-20,582,527 , NCBI36 chr17: 16,557,553-20,426,432 , GRCh37 chr17: 16,616,828-20,485,840 RPL7AP65, EPN2-IT1, 162 more genes
    nsv3924631copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,543,855-20,272,197 , GRCh37 chr17: 16,603,130-20,331,605 , GRCh38 chr17: 16,699,816-20,428,292 EPN2-AS1, RNU6-468P, 148 more genes
    nsv3924307copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,522,249-20,404,912 , GRCh37.p13 chr17: 16,581,524-20,464,320 , GRCh38.p12 chr17: 16,678,210-20,561,007 TOM1L2, USP32P2, 161 more genes
    nsv3924188copy number variation1nstd102humanPathogenic GRCh38 chr17: 16,879,232-18,970,941 , NCBI36 chr17: 16,723,271-18,814,979 , GRCh37 chr17: 16,782,546-18,874,254 LOC107984989, FAM83G, 80 more genes
    nsv3924079copy number variation1nstd102humanPathogenic GRCh38 chr17: 16,836,827-20,465,067 , GRCh37 chr17: 16,740,141-20,368,380 , NCBI36 chr17: 16,680,866-20,308,972 LOC441784, SNORA59B, 139 more genes
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