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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
    nsv7077532inversion1nstd229human GRCh38 chr17: 17,907,928-18,966,216 , GRCh37.p13 chr17: 17,811,242-18,869,529 SMCR8, PAIP1P2, 51 more genes
    nsv7076280inversion1nstd229human GRCh38 chr17: 18,608,940-18,821,521 , GRCh37.p13 chr17: 18,512,253-18,724,834 TRIM16L, LOC107985051, 8 more genes
    nsv7073439inversion1nstd229human GRCh38 chr17: 15,962,151-19,146,977 , GRCh37.p13 chr17: 15,865,465-19,050,290 RNU6-767P, KRT17P5, 129 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
    nsv7063500inversion1nstd229human GRCh38 chr17: 18,620,305-18,830,721 , GRCh37.p13 chr17: 18,523,618-18,734,034 TBC1D28, PAIP1P2, 7 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
    nsv6993579copy number variation1nstd229human GRCh38 chr17: 18,777,761-18,777,841 , GRCh37.p13 chr17: 18,681,074-18,681,154 FBXW10
    nsv6980456copy number variation1nstd229human GRCh38 chr17: 18,769,738-18,769,775 , GRCh37.p13 chr17: 18,673,051-18,673,088 FBXW10
    nsv6637783copy number variation1nstd102humanUncertain significance GRCh37 chr17: 18,599,744-18,882,395 , GRCh38.p12 chr17: 18,696,431-18,979,082 FBXW10, RN7SL627P, 7 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
    nsv6624053copy number variation1nstd224human GRCh37 chr17: 18,602,476-18,875,062 , GRCh38.p12 chr17: 18,699,163-18,971,749 PRPSAP2, FBXW10, 7 more genes
    nsv6624052copy number variation1nstd224human GRCh37 chr17: 18,541,626-18,923,818 , GRCh38.p12 chr17: 18,638,313-19,020,505 FOXO3B, PRPSAP2, 13 more genes
    nsv6624051copy number variation1nstd224human GRCh37 chr17: 18,408,965-18,923,818 , GRCh38.p12 chr17: 18,505,651-19,020,505 GRAP, SLC5A10, 19 more genes
    nsv6624017copy number variation1nstd224human GRCh37 chr17: 18,155,870-18,702,230 , GRCh38.p12 chr17: 18,252,556-18,798,917 SHMT1, SRP68P2, 33 more genes
    nsv6593366inversion1nstd223human GRCh38 chr17: 15,604,136-18,759,631 , GRCh37.p13 chr17: 15,507,450-18,662,944 EEF1A1P43, ZNF624, 131 more genes
    nsv6583947inversion1nstd223human GRCh38 chr17: 18,759,202-18,759,762 , GRCh37.p13 chr17: 18,662,515-18,663,075 FBXW10
    nsv6578694inversion1nstd223human GRCh38 chr17: 15,604,091-18,759,630 , GRCh37.p13 chr17: 15,507,405-18,662,943 TRPV2, SNORD49B, 131 more genes
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