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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3206203copy number variation1estd209human GRCh37 chr17: 32,582,997-32,583,011 , GRCh38.p12 chr17: 34,255,978-34,255,992 CCL2
    esv3371189copy number variation2estd59human NCBI36 chr17: 29,607,094-29,607,834 , GRCh37.p13 chr17: 32,582,981-32,583,721 , GRCh38.p12 chr17: 34,255,962-34,256,702 CCL2
    esv2383370copy number variation1estd194human NCBI36 chr17: 29,607,111-29,607,125 , GRCh37.p13 chr17: 32,582,998-32,583,012 , GRCh38.p12 chr17: 34,255,979-34,255,993 CCL2
    esv3786710tandem duplication1estd192human GRCh37 chr17: 32,582,772-32,586,762 , GRCh38.p12 chr17: 34,255,753-34,259,743 CCL2
    esv3356322insertion1estd59human NCBI36 chr17: 29,608,403-29,608,468 , GRCh37.p13 chr17: 32,584,290-32,584,355 , GRCh38.p12 chr17: 34,257,271-34,257,336 CCL2
    esv3308498mobile element insertion1estd59human NCBI36 chr17: 29,608,412-29,608,458 , GRCh37.p13 chr17: 32,584,299-32,584,345 , GRCh38.p12 chr17: 34,257,280-34,257,326 CCL2
    nsv4242282copy number variation1nstd166human GRCh37.p13 chr17: 32,582,601-32,597,599 , GRCh38.p12 chr17: 34,255,582-34,270,580 CCL2, CCL7
    nsv3168363copy number variation1nstd158human GRCh37 chr17: 32,537,647-32,620,452 , GRCh38.p12 chr17: 34,210,628-34,293,433 CCL2, CCL7, 1 more genes
    nsv3156404copy number variation1nstd151human GRCh37 chr17: 32,582,366-32,647,931 , GRCh38.p12 chr17: 34,255,347-34,320,912 CCL2, CCL8, 2 more genes
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 CCL2, PSMD11, 117 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 CCL2, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 CCL2, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 CCL2, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 CCL2, SMURF2, 2366 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 CCL2, LOC105371922, 1855 more genes
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 CCL2, LOC105371753, 474 more genes
    nsv3910771copy number variation1nstd102humanLikely benign GRCh37 chr17: 31,998,116-32,923,001 , GRCh38 chr17: 33,671,097-34,595,982 , NCBI36 chr17: 29,022,229-29,947,114 CCL2, TMEM132E-DT, 17 more genes
    nsv3917235copy number variation1nstd102humanLikely benign GRCh37 chr17: 31,998,125-32,922,906 , GRCh38 chr17: 33,671,106-34,595,887 , NCBI36 chr17: 29,022,238-29,947,019 CCL2, LOC107987247, 17 more genes
    nsv3907376copy number variation1nstd102humanUncertain significance GRCh37 chr17: 32,351,496-34,455,576 , GRCh38.p12 chr17: 34,024,477-35,919,248 CCL2, CCL8, 67 more genes
    nsv4436271copy number variation1nstd102humanUncertain significance GRCh37 chr17: 31,889,285-33,557,612 , GRCh38.p12 chr17: 33,562,266-35,230,593 CCL2, LOC105371739, 33 more genes
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