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Items: 1 to 20 of 121

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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
    nsv6865837copy number variation1nstd229human GRCh38 chr9: 76,395,972-76,404,289 , GRCh37.p13 chr9: 79,010,888-79,019,205 RPSAP9
    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
    nsv5480328copy number variation1nstd206human GRCh38 chr9: 76,398,626-76,398,690 , GRCh37.p13 chr9: 79,013,542-79,013,606 RPSAP9
    nsv4552239insertion1nstd166human GRCh37.p13 chr9: 79,013,159-79,013,159 , GRCh38.p12 chr9: 76,398,243-76,398,243 RPSAP9
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456241copy number variation1nstd102humanUncertain significance GRCh37 chr9: 78,787,760-79,180,790 , GRCh38.p12 chr9: 76,172,844-76,565,874 RBM22P5, GCNT1, 6 more genes
    nsv4455928copy number variation1nstd102humanPathogenic GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877 RPL35AP21, LOC105376097, 134 more genes
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