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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6875546copy number variation1nstd229human GRCh38 chr9: 76,331,676-76,580,640 , GRCh37.p13 chr9: 78,946,592-79,195,556 PCSK5, RPSAP9, 5 more genes
    nsv6872827copy number variation1nstd229human GRCh38 chr9: 76,174,650-76,561,341 , GRCh37.p13 chr9: 78,789,566-79,176,257 H3P32, PPIAP87, 6 more genes
    nsv6867340copy number variation1nstd229human GRCh38 chr9: 76,333,158-76,409,748 , GRCh37.p13 chr9: 78,948,074-79,024,664 RFK, PCSK5, 1 more genes
    nsv6858847copy number variation1nstd229human GRCh38 chr9: 76,382,198-76,385,691 , GRCh37.p13 chr9: 78,997,114-79,000,607 RFK
    nsv6858520copy number variation1nstd229human GRCh38 chr9: 76,304,337-76,400,613 , GRCh37.p13 chr9: 78,919,253-79,015,529 RPSAP9, RFK, 1 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
    nsv6566822inversion1nstd223human GRCh38 chr9: 75,204,344-76,674,377 , GRCh37.p13 chr9: 77,819,260-79,289,293 RBM22P5, LOC105376091, 11 more genes
    nsv6557715inversion1nstd223human GRCh38 chr9: 75,901,418-82,872,806 , GRCh37.p13 chr9: 78,516,334-85,487,721 , LOC105376096, 79 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
    nsv6314023copy number variation1nstd102humanUncertain significance GRCh37 chr9: 78,824,128-79,392,249 , GRCh38.p12 chr9: 76,209,212-76,777,333 RFK, H3P32, 9 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
    nsv6313827copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484 RPSAP75, ANKRD20A2P, 1008 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
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6136396copy number variation1nstd213human GRCh37 chr9: 78,870,000-79,640,001 , GRCh38.p12 chr9: 76,255,084-77,025,085 RFK, RBM22P5, 11 more genes
    nsv6085348insertion1nstd212human GRCh38 chr9: 76,394,547-76,394,547 , GRCh37.p13 chr9: 79,009,463-79,009,463 RFK
    nsv5542932insertion1nstd206human GRCh38 chr9: 76,394,568-76,394,593 , GRCh37.p13 chr9: 79,009,484-79,009,509 RFK
    nsv4814117copy number variation1nstd200human GRCh37 chr9: 78,998,752-78,998,841 , GRCh38.p12 chr9: 76,383,836-76,383,925 RFK
    nsv4720813insertion1nstd186human GRCh37 chr9: 79,009,458-79,009,458 , GRCh38.p12 chr9: 76,394,542-76,394,542 RFK
    nsv4614528copy number variation1nstd183human GRCh37 chr9: 79,000,505-79,001,501 , GRCh38.p12 chr9: 76,385,589-76,386,585 RFK
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