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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933579copy number variation1nstd209human GRCh38 chr17: 16,936,959-20,558,118 , GRCh37.p13 chr17: 16,840,273-20,461,431 , FAM106B, 146 more genes
    nsv5929989copy number variation1nstd209human GRCh38 chr17: 19,354,807-19,355,812 , GRCh37.p13 chr17: 19,258,120-19,259,125 B9D1
    nsv5670902inversion1nstd207human GRCh37.p13 chr17: 19,143,942-21,250,947 , GRCh38 chr17: 19,240,629-21,558,840 , ALDH3A1, 86 more genes
    nsv5519464copy number variation1nstd206human GRCh38 chr17: 19,358,584-19,362,920 , GRCh37.p13 chr17: 19,261,897-19,266,233 LOC105371573, B9D1
    nsv5381800copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,601,603-20,063,369 , GRCh38.p12 chr17: 16,698,289-20,160,056 COTL1P1, LOC105371551, 141 more genes
    nsv5381797copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,145,361-20,137,943 , GRCh38.p12 chr17: 17,242,047-20,234,630 LOC644909, FLII, 117 more genes
    nsv5026179copy number variation1nstd200human GRCh38 chr17: 19,375,380-19,376,233 , GRCh37.p13 chr17: 19,278,693-19,279,546 MAPK7, B9D1
    nsv5026178copy number variation1nstd200human GRCh38 chr17: 19,339,980-19,342,760 , GRCh37.p13 chr17: 19,243,293-19,246,073 B9D1, MIR1180
    nsv5023745copy number variation1nstd200human GRCh38 chr17: 19,350,371-19,355,889 , GRCh37.p13 chr17: 19,253,684-19,259,202 B9D1
    nsv4864566copy number variation1nstd200human GRCh37 chr17: 19,253,684-19,259,202 , GRCh38.p12 chr17: 19,350,371-19,355,889 B9D1
    nsv4858294copy number variation1nstd200human GRCh37 chr17: 19,276,047-19,278,946 , GRCh38.p12 chr17: 19,372,734-19,375,633 B9D1
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729895copy number variation1nstd102humanUncertain significance GRCh37 chr17: 18,746,987-20,231,379 , GRCh38.p12 chr17: 18,843,674-20,328,066 NDUFB4P3, SNORD3A, 52 more genes
    nsv4729886copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,763,370-20,395,611 , GRCh38.p12 chr17: 16,860,056-20,492,298 LOC100419620, PAIP1P2, 139 more genes
    nsv4729810copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,761,814-20,330,062 , GRCh38.p12 chr17: 16,858,500-20,426,749 PRPSAP2, EPN2, 134 more genes
    nsv4624188copy number variation1nstd183human GRCh37 chr17: 19,145,948-19,352,628 , GRCh38.p12 chr17: 19,242,635-19,449,315 B9D1, EPN2-AS1, 10 more genes
    nsv4349342copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,842,991-20,217,316 , GRCh38.p12 chr17: 16,939,677-20,314,003 LOC105371566, LOC105371569, 126 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4247486copy number variation1nstd166human GRCh37.p13 chr17: 19,275,000-19,286,100 , GRCh38.p12 chr17: 19,371,687-19,382,787 LOC105371573, MAPK7, 2 more genes
    nsv4236910copy number variation1nstd166human GRCh37.p13 chr17: 19,240,784-19,240,837 , GRCh38.p12 chr17: 19,337,471-19,337,524 B9D1
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