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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072948inversion1nstd229human GRCh38 chr9: 86,379,198-87,180,786 , GRCh37.p13 chr9: 88,994,113-89,795,701 GAS1, LINC02893, 8 more genes
    nsv7070278inversion1nstd229human GRCh38 chr9: 85,364,427-88,288,635 , GRCh37.p13 chr9: 87,979,342-90,903,550 LOC105376121, CTSL3P, 57 more genes
    nsv7069712inversion1nstd229human GRCh38 chr9: 85,876,416-87,369,299 , GRCh37.p13 chr9: 88,491,331-89,984,214 CDC20P1, C9orf153, 20 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
    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
    nsv6861841copy number variation1nstd229human GRCh38 chr9: 86,454,606-87,636,718 , GRCh37.p13 chr9: 89,069,521-90,251,633 DAPK1-IT1, CDC20P1, 12 more genes
    nsv6637916copy number variation1nstd102humanUncertain significance GRCh37 chr9: 89,359,204-89,868,057 , GRCh38.p12 chr9: 86,744,289-87,253,142 LOC105376126, GAS1RR, 5 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
    nsv6568042inversion1nstd223human GRCh38 chr9: 77,399,209-87,276,767 , GRCh37.p13 chr9: 80,014,125-89,891,682 , LOC105376119, 118 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
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv5865094copy number variation1nstd209human GRCh38 chr9: 87,139,644-87,149,531 , GRCh37.p13 chr9: 89,754,559-89,764,446 LINC02872
    nsv5858278copy number variation1nstd209human GRCh38 chr9: 87,151,432-87,156,914 , GRCh37.p13 chr9: 89,766,347-89,771,829 LINC02872
    nsv5476151copy number variation1nstd206human GRCh38 chr9: 87,159,176-87,159,409 , GRCh37.p13 chr9: 89,774,091-89,774,324 LINC02872
    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
    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
    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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