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Items: 1 to 20 of 234

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7098895copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,004,894-7,766,789 , GRCh38.p12 chr17: 7,101,575-7,863,471 LOC105371512, EIF4A1, 61 more genes
    nsv7098770copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 7,584,834-7,594,887 , GRCh38.p12 chr17: 7,681,516-7,691,569 TP53, WRAP53
    nsv7095414copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,123,304-8,193,254 , GRCh38.p12 chr17: 7,219,985-8,289,936 CTC1, SAT2, 103 more genes
    nsv7095413copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,123,304-7,606,804 , GRCh38.p12 chr17: 7,219,985-7,703,486 MPDU1, PLSCR3, 50 more genes
    nsv7095410copy number variation2nstd102humanUncertain significance GRCh37 chr17: 6,328,780-7,606,804 , GRCh38.p12 chr17: 6,425,460-7,703,486 PITPNM3, SLC2A4, 85 more genes
    nsv7095366copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,578,129-7,606,804 , GRCh38.p12 chr17: 7,674,811-7,703,486 EFNB3, TP53, 1 more genes
    nsv7095365copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,571,752-8,285,628 , GRCh38.p12 chr17: 7,668,434-8,382,310 TRK-TTT3-5, WRAP53, 59 more genes
    nsv7094990copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,589,449-7,593,039 , GRCh38.p12 chr17: 7,686,131-7,689,721 WRAP53, TP53
    nsv7094989copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,571,752-7,593,029 , GRCh38.p12 chr17: 7,668,434-7,689,711 TP53, WRAP53
    nsv7094920copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,590,130-7,598,840 , GRCh38.p12 chr17: 7,686,812-7,695,522 WRAP53, TP53
    nsv7094919copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,572,921-7,591,611 , GRCh38.p12 chr17: 7,669,603-7,688,293 WRAP53, TP53
    nsv7094915copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,120,455-8,151,423 , GRCh38.p12 chr17: 7,217,136-8,248,105 MIR324, SLC2A4, 101 more genes
    nsv7073912inversion1nstd229human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 TNFSF12, SCARNA21, 321 more genes
    nsv7073657inversion1nstd229human GRCh38 chr17: 3,848,628-8,774,303 , GRCh37.p13 chr17: 3,751,922-8,677,621 LOC107987245, TRI-AAT5-5, 243 more genes
    nsv6985492copy number variation1nstd229human GRCh38 chr17: 7,686,273-7,686,686 , GRCh37.p13 chr17: 7,589,591-7,590,004 WRAP53, TP53
    nsv6982129copy number variation1nstd229human GRCh38 chr17: 7,678,101-7,685,800 , GRCh37.p13 chr17: 7,581,419-7,589,118 TP53, WRAP53
    nsv6637360copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,381,537-8,068,400 , GRCh38.p12 chr17: 7,478,218-8,165,082 LOC107985075, TRT-AGT5-1, 53 more genes
    nsv6591119inversion1nstd223human GRCh38 chr17: 5,860,086-7,699,509 , GRCh37.p13 chr17: 5,763,406-7,602,827 RPL23AP73, MIR195, 90 more genes
    nsv6589878inversion1nstd223human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 ASGR1, KIF1C-AS1, 321 more genes
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