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Items: 1 to 20 of 413

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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
    nsv7095135copy number variation1nstd102humanPathogenic GRCh37 chr17: 19,575,024-19,575,279 , GRCh38.p12 chr17: 19,671,711-19,671,966 ALDH3A2
    nsv7095134copy number variation1nstd102humanPathogenic GRCh37 chr17: 19,552,285-19,561,195 , GRCh38.p12 chr17: 19,648,972-19,657,882 ALDH3A2
    nsv7095081copy number variation1nstd102humanPathogenic GRCh37 chr17: 19,554,850-19,555,955 , GRCh38.p12 chr17: 19,651,537-19,652,642 ALDH3A2
    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
    nsv7094960copy number variation1nstd102humanPathogenic GRCh37 chr17: 19,564,420-19,564,601 , GRCh38.p12 chr17: 19,661,107-19,661,288 ALDH3A2
    nsv7094863copy number variation1nstd102humanPathogenic GRCh37 chr17: 19,559,659-19,568,380 , GRCh38.p12 chr17: 19,656,346-19,665,067 ALDH3A2
    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
    nsv7077458inversion1nstd229human GRCh38 chr17: 19,655,327-19,749,869 , GRCh37.p13 chr17: 19,558,640-19,653,182 SLC47A2, ALDH3A2, 1 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
    nsv6998082copy number variation1nstd229human GRCh38 chr17: 19,654,501-19,658,600 , GRCh37.p13 chr17: 19,557,814-19,561,913 ALDH3A2
    nsv6997683copy number variation1nstd229human GRCh38 chr17: 19,662,495-19,905,171 , GRCh37.p13 chr17: 19,565,808-19,808,484 ULK2, NDUFB4P3, 6 more genes
    nsv6991302copy number variation1nstd229human GRCh38 chr17: 19,519,452-19,681,956 , GRCh37.p13 chr17: 19,422,765-19,585,269 SLC47A1, NMTRQ-TTG12-1, 8 more genes
    nsv6988503copy number variation1nstd229human GRCh38 chr17: 19,668,598-19,669,009 , GRCh37.p13 chr17: 19,571,911-19,572,322 ALDH3A2
    nsv6987641copy number variation1nstd229human GRCh38 chr17: 19,671,957-19,675,560 , GRCh37.p13 chr17: 19,575,270-19,578,873 ALDH3A2
    nsv6981567copy number variation1nstd229human GRCh38 chr17: 19,655,301-19,708,700 , GRCh37.p13 chr17: 19,558,614-19,612,013 ALDH3A2, SLC47A2
    nsv6637475copy number variation1nstd102humanUncertain significance GRCh37 chr17: 19,423,469-19,588,176 , GRCh38.p12 chr17: 19,520,156-19,684,863 MTND2P12, SNORA59B, 8 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
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