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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
    nsv6137704copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,426,622-38,787,479 , GRCh38.p12 chr9: 36,426,625-38,787,482 MELK, SLC25A51, 55 more genes
    nsv6137700copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,088,563-39,092,820 , GRCh38.p12 chr9: 36,088,566-39,092,823 SNX18P3, VN1R48P, 69 more genes
    nsv4964421copy number variation1nstd200human GRCh38 chr9: 38,410,463-38,420,778 , GRCh37.p13 chr9: 38,410,460-38,420,775 IGFBPL1
    nsv4954693copy number variation1nstd200human GRCh38 chr9: 38,402,197-38,409,698 , GRCh37.p13 chr9: 38,402,194-38,409,695 IGFBPL1
    nsv4828332copy number variation1nstd200human GRCh37 chr9: 38,410,488-38,420,779 , GRCh38.p12 chr9: 38,410,491-38,420,782 IGFBPL1
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4728775copy number variation1nstd102humanLikely benign GRCh37 chr9: 38,300,619-38,498,138 , GRCh38.p12 chr9: 38,300,622-38,498,141 ALDH1B1, TCEA1P3, 5 more genes
    nsv4680652copy number variation1nstd189human GRCh37.p13 chr9: 38,189,524-38,420,501 , GRCh38.p12 chr9: 38,189,527-38,420,504 ALDH1B1, IGFBPL1, 3 more genes
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4675481copy number variation1nstd102humanUncertain significance GRCh37 chr9: 36,539,229-38,787,480 , GRCh38.p12 chr9: 36,539,232-38,787,483 LOC105376042, CYP4F33P, 54 more genes
    nsv4544022insertion1nstd166human GRCh37.p13 chr9: 38,411,097-38,411,097 , GRCh38.p12 chr9: 38,411,100-38,411,100 IGFBPL1
    nsv4540988insertion1nstd166human GRCh37.p13 chr9: 38,411,147-38,411,147 , GRCh38.p12 chr9: 38,411,150-38,411,150 IGFBPL1
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4457200copy number variation2nstd102humanPathogenic GRCh37 chr9: 203,861-67,986,965 , GRCh38.p12 chr9: 203,861-67,919,519 ACO1, RNU6-1073P, 846 more genes
    nsv4456028copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-38,472,979 , GRCh38.p12 chr9: 203,861-38,472,982 SNORA30B, LOC100419692, 559 more genes
    nsv4455152copy number variation1nstd102humanPathogenic GRCh37 chr9: 34,542,635-68,210,033 , GRCh38.p12 chr9: 34,542,637-67,920,552 FAM74A6, RGP1, 415 more genes
    nsv4436161complex substitution1nstd102humanLikely pathogenic GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888 ACO1, ALDH1A1, 779 more genes
    nsv4365194copy number variation1nstd173human GRCh37 chr9: 38,362,633-38,771,831 , GRCh38.p12 chr9: 38,362,636-38,771,834 LOC105376040, FAM201A, 15 more genes
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