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Items: 1 to 20 of 316

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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
    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
    nsv6142618copy number variation1nstd206human GRCh38 chr9: 65,282,000-65,296,082 , GRCh37.p13 chr9: 70,175,606-70,189,688 ZNG1DP, FOXD4L5
    nsv6142000copy number variation1nstd206human GRCh38 chr9: 65,262,000-65,324,200 , GRCh37.p13 chr9: 70,155,606-70,217,806 FOXD4L5, ZNG1DP
    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
    nsv5919501copy number variation1nstd209human GRCh38 chr9: 61,557,000-65,487,786 , GRCh37.p13 chr: NaN-NaN , MTCO1P36, 98 more genes
    nsv5918216copy number variation1nstd209human GRCh38 chr9: 61,647,960-65,578,967 , GRCh37.p13 chr: NaN-NaN , SDR42E1P3, 99 more genes
    nsv5914346copy number variation1nstd209human GRCh38 chr9: 60,768,680-66,674,368 , GRCh37.p13 chr: NaN-NaN , MEP1AP3, 146 more genes
    nsv5910323copy number variation1nstd209human GRCh38 chr9: 61,604,972-65,538,433 , GRCh37.p13 chr: NaN-NaN , FAM242E, 98 more genes
    nsv5259273copy number variation1nstd204human GRCh38.p13 chr9: 65,267,501-65,291,100 , GRCh37.p13 chr9: 70,161,107-70,184,706 FOXD4L5, ZNG1DP
    nsv5258889copy number variation1nstd204human GRCh38.p13 chr9: 65,277,401-65,282,800 , GRCh37.p13 chr9: 70,171,007-70,176,406 FOXD4L5
    nsv5258874copy number variation1nstd204human GRCh38.p13 chr9: 65,276,001-65,281,800 , GRCh37.p13 chr9: 70,169,607-70,175,406 FOXD4L5
    nsv5258508copy number variation1nstd204human GRCh38.p13 chr9: 65,282,001-65,282,800 , GRCh37.p13 chr9: 70,175,607-70,176,406 FOXD4L5
    nsv5257780copy number variation1nstd204human GRCh38.p13 chr9: 65,280,201-65,281,400 , GRCh37.p13 chr9: 70,173,807-70,175,006 FOXD4L5
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