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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070730inversion1nstd229human GRCh38 chr9: 62,058,130-67,204,238 , GRCh37.p13 chr9: 41,204,320-44,676,072 ATP5F1AP10, IGKV1OR9-1, 125 more genes
    nsv7064084inversion1nstd229human GRCh38 chr9: 64,120,773-68,530,496 , GRCh37.p13 chr9: 40,041,911-44,672,613 LOC112267859, ZNG1C, 91 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
    nsv6454154copy number variation1nstd223human GRCh38 chr9: 65,712,601-65,740,100 , GRCh37.p13 chr9: 70,425,945-70,453,444 FOXD4L4, ZNG1E
    nsv6453722copy number variation1nstd223human GRCh38 chr9: 65,645,301-65,775,000 , GRCh37.p13 chr9: 70,391,045-70,504,506 ZNG1E, FOXD4L4, 1 more genes
    nsv6453182copy number variation1nstd223human GRCh38 chr9: 65,704,901-65,743,700 , GRCh37.p13 chr9: 70,422,345-70,461,144 ZNG1E, FOXD4L4
    nsv6449039copy number variation1nstd223human GRCh38 chr9: 65,706,601-65,739,900 , GRCh37.p13 chr9: 70,426,145-70,459,444 ZNG1E, FOXD4L4
    nsv6444650copy number variation1nstd223human GRCh38 chr9: 65,703,501-65,745,700 , GRCh37.p13 chr9: 70,420,345-70,462,544 ZNG1E, FOXD4L4
    nsv6444434copy number variation1nstd223human GRCh38 chr9: 65,707,701-65,743,600 , GRCh37.p13 chr9: 70,422,445-70,458,344 ZNG1E, FOXD4L4
    nsv6441353copy number variation1nstd223human GRCh38 chr9: 65,738,701-65,742,000 , GRCh37.p13 chr9: 70,424,045-70,427,344 FOXD4L4
    nsv6441039copy number variation1nstd223human GRCh38 chr9: 65,728,701-65,748,200 , GRCh37.p13 chr9: 70,417,845-70,437,344 FOXD4L4, ZNG1E
    nsv6438443copy number variation1nstd223human GRCh38 chr9: 65,721,301-65,745,400 , GRCh37.p13 chr9: 70,420,645-70,444,744 ZNG1E, FOXD4L4
    nsv6315415copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552 LOC107987068, FAM74A7, 846 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
    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
    nsv6142863copy number variation1nstd206human GRCh38 chr9: 65,657,191-66,049,191 , GRCh37.p13 chr9: 42,827,894-43,029,769 , LOC100132599, 15 more genes
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
    nsv5978274inversion1nstd209human GRCh38 chr9: 65,735,736-66,185,775 , GRCh37.p13 chr9: 42,827,894-43,166,353 , FOXD4L4, 17 more genes
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