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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070278inversion1nstd229human GRCh38 chr9: 85,364,427-88,288,635 , GRCh37.p13 chr9: 87,979,342-90,903,550 LOC105376121, CTSL3P, 57 more genes
    nsv7070039inversion1nstd229human GRCh38 chr9: 87,255,950-90,941,993 , GRCh37.p13 chr9: 89,870,865-93,704,275 LOC389768, RPS10P3, 69 more genes
    nsv7068881inversion1nstd229human GRCh38 chr9: 85,364,378-88,276,332 , GRCh37.p13 chr9: 87,979,293-90,891,247 LOC100129202, LOC100287212, 57 more genes
    nsv7059923inversion1nstd229human GRCh38 chr9: 87,301,614-87,977,114 , GRCh37.p13 chr9: 89,916,529-90,592,029 CTSL, LOC105376131, 21 more genes
    nsv6876414copy number variation1nstd229human GRCh38 chr9: 87,623,057-88,194,238 , GRCh37.p13 chr9: 90,237,972-90,809,153 DAPK1, RNU6-86P, 24 more genes
    nsv6862777copy number variation1nstd229human GRCh38 chr9: 86,566,451-88,481,061 , GRCh37.p13 chr9: 89,181,366-91,095,976 CTSL3P, CTSLP8, 40 more genes
    nsv6860213copy number variation1nstd229human GRCh38 chr9: 87,659,758-87,840,418 , GRCh37.p13 chr9: 90,274,673-90,455,333 EIF3JP3, LOC100420576, 6 more genes
    nsv6637616copy number variation1nstd102humanUncertain significance GRCh37 chr9: 90,266,171-90,565,780 , GRCh38.p12 chr9: 87,651,256-87,950,865 FBP2P1, SPATA31C1, 15 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291242copy number variation1nstd102humanUncertain significance GRCh37 chr9: 90,336,741-90,609,494 , GRCh38.p12 chr9: 87,721,826-87,994,579 NPAP1P7, CTSL3P, 16 more genes
    nsv6290258copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 90,342,469-93,657,932 , GRCh38.p12 chr9: 87,727,554-90,895,650 CKS2, CTSL, 61 more genes
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv5487993copy number variation1nstd206human GRCh38 chr9: 87,834,218-87,837,085 , GRCh37.p13 chr9: 90,449,133-90,452,000 FBP2P1
    nsv4729544copy number variation1nstd102humanUncertain significance GRCh37 chr9: 90,353,229-90,514,102 , GRCh38.p12 chr9: 87,738,314-87,899,187 NPAP1P5, LOC112267903, 11 more genes
    nsv4729419copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 90,031,614-93,173,691 , GRCh38.p12 chr9: 87,416,699-90,411,409 CKS2, CTSL, 60 more genes
    nsv4680900copy number variation1nstd189human GRCh37.p13 chr9: 90,185,615-90,731,440 , GRCh38.p12 chr9: 87,570,700-88,116,525 CTSL, CTSLP8, 20 more genes
    nsv4680239copy number variation1nstd189human GRCh37.p13 chr9: 90,201,816-90,722,897 , GRCh38.p12 chr9: 87,586,901-88,107,982 CTSL, CTSLP8, 20 more genes
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