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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 PSMD11, C17orf50, 117 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6998019copy number variation1nstd229human GRCh38 chr17: 32,982,862-32,993,435 , GRCh37.p13 chr17: 31,309,880-31,320,453 SPACA3
    nsv6993616copy number variation1nstd229human GRCh38 chr17: 32,993,657-32,994,257 , GRCh37.p13 chr17: 31,320,675-31,321,275 SPACA3
    nsv6987432copy number variation1nstd229human GRCh38 chr17: 32,993,610-32,993,708 , GRCh37.p13 chr17: 31,320,628-31,320,726 SPACA3
    nsv6983842copy number variation1nstd229human GRCh38 chr17: 32,982,820-33,007,809 , GRCh37.p13 chr17: 31,309,838-31,334,827 SPACA3
    nsv6500513copy number variation1nstd223human GRCh38 chr17: 32,993,676-32,994,355 , GRCh37.p13 chr17: 31,320,694-31,321,373 SPACA3
    nsv6133300copy number variation1nstd213human GRCh37 chr17: 30,620,000-31,340,001 , GRCh38.p12 chr17: 32,292,981-33,012,983 ASIC2, MYO1D, 13 more genes
    nsv6133238copy number variation1nstd213human GRCh37 chr17: 30,800,000-31,380,001 , GRCh38.p12 chr17: 32,472,982-33,052,983 ASIC2, MYO1D, 7 more genes
    nsv6133229copy number variation1nstd213human GRCh37 chr17: 25,300,000-32,120,001 , GRCh38.p12 chr17: 26,972,974-33,792,982 BLMH, CPD, 197 more genes
    nsv5932495copy number variation1nstd209human GRCh38 chr17: 32,996,530-32,996,612 , GRCh37.p13 chr17: 31,323,548-31,323,630 SPACA3
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5520901copy number variation1nstd206human GRCh38 chr17: 32,996,532-32,996,613 , GRCh37.p13 chr17: 31,323,550-31,323,631 SPACA3
    nsv5016081copy number variation1nstd200human GRCh38 chr17: 32,996,532-32,996,613 , GRCh37.p13 chr17: 31,323,550-31,323,631 SPACA3
    nsv5016080copy number variation1nstd200human GRCh38 chr17: 32,993,677-32,994,355 , GRCh37.p13 chr17: 31,320,695-31,321,373 SPACA3
    nsv4858619copy number variation1nstd200human GRCh37 chr17: 31,320,695-31,321,373 , GRCh38.p12 chr17: 32,993,677-32,994,355 SPACA3
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729951copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,989,741-32,355,632 , GRCh38.p12 chr17: 31,662,722-34,028,613 RNA5SP437, PSMD11, 34 more genes
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4384972copy number variation1nstd173human GRCh37 chr17: 27,710,978-33,392,085 , GRCh38.p12 chr17: 29,383,960-35,065,066 , LOC105371737, 137 more genes
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