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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929452copy number variation1nstd209human GRCh38 chr17: 6,412,133-13,962,466 , GRCh37.p13 chr17: 6,315,453-13,865,783 , PIK3R5-DT, 226 more genes
    nsv5673052copy number variation1nstd102humanPathogenic GRCh37 chr17: 6,589,506-7,128,436 , GRCh38.p12 chr17: 6,686,187-7,225,117 RPL23AP73, MIR195, 25 more genes
    nsv5381181copy number variation1nstd102humanUncertain significance GRCh37 chr17: 6,328,780-7,128,416 , GRCh38.p12 chr17: 6,425,460-7,225,097 RNA5SP435, RPL23AP73, 37 more genes
    nsv5297723copy number variation1nstd204human GRCh38.p13 chr17: 6,724,142-6,757,134 , GRCh37.p13 chr17: 6,627,461-6,660,453 XAF1, RPL23AP73
    nsv5282758copy number variation1nstd204human GRCh38.p13 chr17: 6,759,964-6,761,084 , GRCh37.p13 chr17: 6,663,283-6,664,403 XAF1
    nsv5023610copy number variation1nstd200human GRCh38 chr17: 6,768,144-6,778,985 , GRCh37.p13 chr17: 6,671,463-6,682,304 XAF1, FBXO39
    nsv5023609copy number variation1nstd200human GRCh38 chr17: 6,750,085-6,753,881 , GRCh37.p13 chr17: 6,653,404-6,657,200 RPL23AP73, XAF1
    nsv5015696copy number variation1nstd200human GRCh38 chr17: 6,745,002-6,754,219 , GRCh37.p13 chr17: 6,648,321-6,657,538 RPL23AP73, XAF1
    nsv5015695copy number variation1nstd200human GRCh38 chr17: 6,724,159-6,902,878 , GRCh37.p13 chr17: 6,627,478-6,806,197 FBXO39, RPL23AP73, 3 more genes
    nsv4864490copy number variation1nstd200human GRCh37 chr17: 6,671,463-6,682,304 , GRCh38.p12 chr17: 6,768,144-6,778,985 XAF1, FBXO39
    nsv4864489copy number variation1nstd200human GRCh37 chr17: 6,653,404-6,657,200 , GRCh38.p12 chr17: 6,750,085-6,753,881 RPL23AP73, XAF1
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729929copy number variation1nstd102humanPathogenic GRCh37 chr17: 6,650,649-8,040,151 , GRCh38.p12 chr17: 6,747,330-8,136,833 CYB5D1, GPS2, 98 more genes
    nsv4683612copy number variation2nstd102humanUncertain significance GRCh37 chr17: 6,589,506-8,151,374 , GRCh38.p12 chr17: 6,686,187-8,248,056 ALOX12P2, DLG4, 124 more genes
    nsv4675132copy number variation1nstd102humanUncertain significance GRCh37 chr17: 6,630,435-6,800,894 , GRCh38.p12 chr17: 6,727,116-6,897,575 FBXO39, TEKT1, 3 more genes
    nsv4344273sequence alteration1nstd166human GRCh37.p13 chr17: 6,626,522-6,806,197 , GRCh38.p12 chr17: 6,723,203-6,902,878 ALOX12P2, XAF1, 3 more genes
    nsv4234577copy number variation1nstd166human GRCh37.p13 chr17: 6,662,297-6,662,354 , GRCh38.p12 chr17: 6,758,978-6,759,035 XAF1
    nsv3936153copy number variation1nstd167human GRCh37 chr17: 6,661,683-6,661,731 , GRCh38.p12 chr17: 6,758,364-6,758,412 XAF1
    nsv3923152copy number variation1nstd102humanPathogenic NCBI36 chr17: 3,451,558-7,022,067 , GRCh38 chr17: 3,601,515-7,178,024 , GRCh37 chr17: 3,504,809-7,081,343 PSMB6, NUP88, 133 more genes
    nsv3917777copy number variation1nstd102humanPathogenic GRCh37 chr17: 50,690-7,394,448 , GRCh38 chr17: 198,748-7,491,129 , NCBI36 chr17: 48,539-7,335,172 PAFAH1B1, PELP1-DT, 267 more genes
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