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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5934993copy number variation1nstd209human GRCh38 chr17: 7,571,836-7,571,888 , GRCh37.p13 chr17: 7,475,154-7,475,206 EIF4A1, SENP3, 1 more genes
    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
    nsv5601596copy number variation1nstd207human GRCh38 chr17: 7,571,846-7,571,911 , GRCh37.p13 chr17: 7,475,164-7,475,229 EIF4A1, SENP3, 1 more genes
    nsv5518154copy number variation1nstd206human GRCh38 chr17: 7,200,922-7,654,532 , GRCh37.p13 chr17: 7,104,241-7,557,850 SNORA48, MPDU1-AS1, 47 more genes
    nsv5358610translocation1nstd200human GRCh38 chr17: 7,579,322-7,579,322 , GRCh38 chr17: 7,579,612-7,579,612 , GRCh37.p13 chr17: 7,482,640-7,482,640 , GRCh37.p13 chr17: 7,482,930-7,482,930 CD68, EIF4A1, 1 more genes
    nsv5295633copy number variation1nstd204human GRCh38.p13 chr17: 7,571,601-7,692,600 , GRCh37.p13 chr17: 7,474,919-7,595,918 MPDU1-AS1, SENP3-EIF4A1, 15 more genes
    nsv5284241copy number variation1nstd204human GRCh38.p13 chr17: 7,363,101-7,796,500 , GRCh37.p13 chr17: 7,266,420-7,699,818 SAT2, TNFSF12, 35 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
    nsv5281320copy number variation1nstd204human GRCh38.p13 chr17: 7,573,240-7,577,595 , GRCh37.p13 chr17: 7,476,558-7,480,913 SNORA48, SENP3-EIF4A1, 3 more genes
    nsv4857948copy number variation1nstd200human GRCh37 chr17: 7,482,640-7,482,930 , GRCh38.p12 chr17: 7,579,322-7,579,612 SENP3-EIF4A1, EIF4A1, 1 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4737564copy number variation1nstd199human GRCh37 chr17: 7,475,167-7,475,224 , GRCh38.p12 chr17: 7,571,849-7,571,906 EIF4A1, SENP3, 1 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
    nsv4675912copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,381,536-7,535,411 , GRCh38.p12 chr17: 7,478,217-7,632,093 ZBTB4, SNORD10, 18 more genes
    nsv4632435copy number variation1nstd183human GRCh37 chr17: 7,482,688-7,482,932 , GRCh38.p12 chr17: 7,579,370-7,579,614 CD68, SENP3-EIF4A1, 1 more genes
    nsv4244919copy number variation1nstd166human GRCh37.p13 chr17: 7,482,640-7,482,930 , GRCh38.p12 chr17: 7,579,322-7,579,612 EIF4A1, SENP3-EIF4A1, 1 more genes
    nsv4243791copy number variation1nstd166human GRCh37.p13 chr17: 7,469,000-7,480,000 , GRCh38.p12 chr17: 7,565,683-7,576,682 EIF4A1, SENP3, 4 more genes
    nsv4243610copy number variation1nstd166human GRCh37.p13 chr17: 7,474,000-7,479,250 , GRCh38.p12 chr17: 7,570,682-7,575,932 EIF4A1, SNORD10, 3 more genes
    nsv3932052copy number variation1nstd167human GRCh37 chr17: 7,475,195-7,475,235 , GRCh38.p12 chr17: 7,571,877-7,571,917 EIF4A1, SENP3, 1 more genes
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