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Items: 1 to 20 of 104

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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
    nsv5555987sequence alteration1nstd206human GRCh38 chr17: 6,997,644-7,111,528 , GRCh37.p13 chr17: 6,900,963-7,014,847 ASGR2, SLC16A11, 11 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
    nsv5283638copy number variation1nstd204human GRCh38.p13 chr17: 6,923,801-7,855,300 , GRCh37.p13 chr17: 6,827,120-7,758,618 , TNFSF12, 74 more genes
    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
    nsv4676022copy number variation1nstd102humanPathogenic GRCh37 chr17: 6,800,893-7,304,696 , GRCh38.p12 chr17: 6,897,574-7,401,377 DVL2, PHF23, 37 more genes
    nsv4630637copy number variation1nstd183human GRCh37 chr17: 6,915,305-6,918,454 , GRCh38.p12 chr17: 7,011,986-7,015,135 C17orf49, RNASEK, 3 more genes
    nsv4457820copy number variation1nstd102humanUncertain significance GRCh37 chr17: 6,826,243-7,311,408 , GRCh38.p12 chr17: 6,922,924-7,408,089 ASGR2, PHF23, 37 more genes
    nsv4249754copy number variation1nstd166human GRCh37.p13 chr17: 6,914,000-6,919,250 , GRCh38.p12 chr17: 7,010,681-7,015,931 ALOX12, C17orf49, 6 more genes
    nsv4241950copy number variation1nstd166human GRCh37.p13 chr17: 6,914,700-6,922,000 , GRCh38.p12 chr17: 7,011,381-7,018,681 C17orf49, MIR195, 5 more genes
    nsv3924691copy number variation1nstd102humanUncertain significance GRCh37 chr17: 6,794,676-7,167,553 , GRCh38 chr17: 6,891,357-7,264,234 , NCBI36 chr17: 6,735,400-7,108,277 ELP5, RNASEK, 25 more genes
    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
    nsv3917059copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901 PSMB6, RNU6-1065P, 409 more genes
    nsv3915354copy number variation1nstd102humanPathogenic GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519 KIF1C-AS1, TMEM107, 433 more genes
    nsv3913013copy number variation1nstd102humanPathogenic GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055 RPS4XP17, SNORA67, 289 more genes
    nsv3911050copy number variation1nstd102humanPathogenic GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391 C17orf49, SPEM1, 209 more genes
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