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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7058413inversion1nstd229human GRCh38 chr9: 78,853,492-79,523,476 , GRCh37.p13 chr9: 81,468,408-82,138,391 KRT18P24, CHCHD2P9, 3 more genes
    nsv6877917copy number variation1nstd229human GRCh38 chr9: 79,134,508-79,134,693 , GRCh37.p13 chr9: 81,749,423-81,749,608 LOC101927450
    nsv6866910copy number variation1nstd229human GRCh38 chr9: 79,141,001-79,148,300 , GRCh37.p13 chr9: 81,755,916-81,763,215 LOC101927450
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6568042inversion1nstd223human GRCh38 chr9: 77,399,209-87,276,767 , GRCh37.p13 chr9: 80,014,125-89,891,682 , LOC105376119, 118 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
    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
    nsv6136845copy number variation1nstd213human GRCh37 chr9: 81,530,000-83,460,001 , GRCh38.p12 chr9: 78,915,084-80,845,086 RPS19P6, NPAP1P6, 15 more genes
    nsv6136397copy number variation1nstd213human GRCh37 chr9: 79,800,000-82,150,001 , GRCh38.p12 chr9: 77,185,084-79,535,086 CHCHD2P9, MTND2P8, 21 more genes
    nsv5036269inversion1nstd200human GRCh38 chr9: 79,108,237-87,224,469 , GRCh37.p13 chr9: 81,723,153-89,839,384 , RMI1, 100 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 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
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4455073copy number variation1nstd102humanUncertain significance GRCh37 chr9: 78,672,613-83,349,616 , GRCh38.p12 chr9: 76,057,697-80,734,701 LOC105376100, NPAP1P6, 49 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
    nsv4349215copy number variation1nstd102humanPathogenic GRCh37 chr9: 79,520,825-97,201,274 , GRCh38.p12 chr9: 76,905,909-94,438,992 SPATA31C1, LINC02893, 280 more genes
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