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Items: 1 to 20 of 258

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137103copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,664,739-20,370,783 , GRCh38.p12 chr17: 16,761,425-20,467,470 NMTRQ-TTG12-1, NOS2P4, 148 more genes
    nsv7098881copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,116,969-20,217,378 , GRCh38.p12 chr17: 17,213,655-20,314,065 LOC105371578, SNORD3B-2, 119 more genes
    nsv7095079copy number variation1nstd102humanUncertain significance GRCh37 chr17: 19,246,632-19,578,885 , GRCh38.p12 chr17: 19,343,319-19,675,572 RPS2P46, LOC105371578, 18 more genes
    nsv7093160copy number variation1nstd102humanPathogenic GRCh38 chr17: 18,856,298-20,402,192 , GRCh37.p13 chr17: 18,759,611-20,305,505 LOC100131943, GRAP, 53 more genes
    nsv7070653inversion1nstd229human GRCh38 chr17: 18,758,972-20,738,114 , GRCh37.p13 chr17: 18,662,285-20,641,427 LOC401875, LGALS9B, 81 more genes
    nsv7061998inversion1nstd229human GRCh38 chr17: 18,691,607-20,798,512 , GRCh37.p13 chr17: 18,594,920-20,701,825 RNU6-467P, SLC47A1P1, 86 more genes
    nsv6997056copy number variation1nstd229human GRCh38 chr17: 19,385,823-19,394,286 , GRCh37.p13 chr17: 19,289,136-19,297,599 MFAP4
    nsv6992761copy number variation1nstd229human GRCh38 chr17: 19,382,946-19,383,078 , GRCh37.p13 chr17: 19,286,259-19,286,391 MFAP4, MAPK7
    nsv6981965copy number variation1nstd229human GRCh38 chr17: 19,384,739-19,387,565 , GRCh37.p13 chr17: 19,288,052-19,290,878 MFAP4
    nsv6981037copy number variation1nstd229human GRCh38 chr17: 19,307,492-19,586,909 , GRCh37.p13 chr17: 19,210,805-19,490,222 LOC105371578, RPL17P43, 14 more genes
    nsv6978503copy number variation1nstd229human GRCh38 chr17: 19,286,558-19,418,187 , GRCh37.p13 chr17: 19,189,871-19,321,500 LOC105371574, EPN2-AS1, 8 more genes
    nsv6637220copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,103,571-19,331,028 , GRCh38.p12 chr17: 17,200,257-19,427,715 PRPSAP2, SNORD3A, 96 more genes
    nsv6634447copy number variation1nstd102humanUncertain significance GRCh37 chr17: 16,736,709-20,339,460 , GRCh38.p12 chr17: 16,833,395-20,436,147 KCTD9P1, MTCO1P39, 139 more genes
    nsv6315482copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,151,140-20,187,953 , GRCh38.p12 chr17: 17,247,826-20,284,640 COPS3, KYNUP2, 116 more genes
    nsv6315475copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,651,292-20,286,898 , GRCh38.p12 chr17: 16,747,978-20,383,585 MIR33B, KRT17P2, 143 more genes
    nsv6315238complex substitution1nstd102humanPathogenic GRCh37 chr17: 14,876,984-22,124,952 , GRCh38.p12 chr17: 14,973,667-22,625,625 ADORA2B, ALDH3A1, 281 more genes
    nsv6314758copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,664,739-20,217,378 , GRCh38.p12 chr17: 16,761,425-20,314,065 EEF1A1P43, LOC105371566, 140 more genes
    nsv6310150copy number variation2nstd102humanUncertain significance GRCh37 chr17: 16,842,861-19,578,885 , GRCh38.p12 chr17: 16,939,547-19,675,572 TSEN15P1, SNORD3A, 114 more genes
    nsv6290324copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,829,153-20,361,747 , GRCh38.p12 chr17: 16,925,839-20,458,434 YWHAEP2, EEF1A1P43, 135 more genes
    nsv6133043copy number variation1nstd213human GRCh37 chr17: 19,110,000-19,370,001 , GRCh38.p12 chr17: 19,206,687-19,466,688 MFAP4, MAPK7, 12 more genes
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