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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
    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
    nsv7067153inversion1nstd229human GRCh38 chr9: 86,191,670-86,625,556 , GRCh37.p13 chr9: 88,806,585-89,240,471 RPS6P13, RN7SKP264, 6 more genes
    nsv6874692copy number variation1nstd229human GRCh38 chr9: 86,274,602-86,278,299 , GRCh37.p13 chr9: 88,889,517-88,893,214 ISCA1
    nsv6871113copy number variation1nstd229human GRCh38 chr9: 86,281,223-86,283,637 , GRCh37.p13 chr9: 88,896,138-88,898,552 ISCA1
    nsv6859814copy number variation1nstd229human GRCh38 chr9: 86,276,501-86,386,000 , GRCh37.p13 chr9: 88,891,416-89,000,915 RPS6P13, TUT7, 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
    nsv6568042inversion1nstd223human GRCh38 chr9: 77,399,209-87,276,767 , GRCh37.p13 chr9: 80,014,125-89,891,682 , LOC105376119, 118 more genes
    nsv6564425inversion1nstd223human GRCh38 chr9: 86,051,015-86,392,968 , GRCh37.p13 chr9: 88,665,930-89,007,883 GOLM1, TUT7, 6 more genes
    nsv6562752inversion1nstd223human GRCh38 chr9: 86,051,014-86,393,052 , GRCh37.p13 chr9: 88,665,929-89,007,967 GOLM1, TUT7, 6 more genes
    nsv6441984copy number variation1nstd223human GRCh38 chr9: 86,262,610-86,263,004 , GRCh37.p13 chr9: 88,877,525-88,877,919 ISCA1
    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
    nsv6279018insertion1nstd214human GRCh38 chr9: 86,278,193-86,278,193 , GRCh37.p13 chr9: 88,893,108-88,893,108 ISCA1
    nsv5920502copy number variation1nstd209human GRCh38 chr9: 86,271,286-86,271,343 , GRCh37.p13 chr9: 88,886,201-88,886,258 ISCA1
    nsv5544838insertion1nstd206human GRCh38 chr9: 86,278,208-86,278,244 , GRCh37.p13 chr9: 88,893,123-88,893,159 ISCA1
    nsv5036269inversion1nstd200human GRCh38 chr9: 79,108,237-87,224,469 , GRCh37.p13 chr9: 81,723,153-89,839,384 , RMI1, 100 more genes
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