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Items: 1 to 20 of 295

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077711inversion1nstd229human GRCh38 chr9: 97,505,240-97,509,856 , GRCh37.p13 chr9: 100,267,522-100,272,138 TMOD1
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv6866679copy number variation1nstd229human GRCh38 chr9: 97,590,341-97,590,478 , GRCh37.p13 chr9: 100,352,623-100,352,760 TMOD1
    nsv6866641copy number variation1nstd229human GRCh38 chr9: 97,577,143-97,577,196 , GRCh37.p13 chr9: 100,339,425-100,339,478 TMOD1
    nsv6861881copy number variation1nstd229human GRCh38 chr9: 97,554,568-97,555,255 , GRCh37.p13 chr9: 100,316,850-100,317,537 TMOD1
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6565428inversion1nstd223human GRCh38 chr9: 97,589,104-97,589,331 , GRCh37.p13 chr9: 100,351,386-100,351,613 TMOD1
    nsv6558935inversion1nstd223human GRCh38 chr9: 97,589,112-97,589,302 , GRCh37.p13 chr9: 100,351,394-100,351,584 TMOD1
    nsv6447907copy number variation1nstd223human GRCh38 chr9: 97,501,401-97,501,800 , GRCh37.p13 chr9: 100,263,683-100,264,082 TMOD1
    nsv6447755copy number variation1nstd223human GRCh38 chr9: 92,901,749-100,255,234 , GRCh37.p13 chr9: 95,664,031-103,017,516 EIF4BP3, VN1R51P, 162 more genes
    nsv6444007copy number variation1nstd223human GRCh38 chr9: 97,547,601-97,550,000 , GRCh37.p13 chr9: 100,309,883-100,312,282 TMOD1
    nsv6436026copy number variation1nstd223human GRCh38 chr9: 97,547,835-97,548,261 , GRCh37.p13 chr9: 100,310,117-100,310,543 TMOD1
    nsv6435687copy number variation1nstd223human GRCh38 chr9: 97,519,305-97,519,701 , GRCh37.p13 chr9: 100,281,587-100,281,983 TMOD1
    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
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 SUGT1P4-STRA6LP, NR4A3, 255 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
    nsv6312742copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 100,190,748-103,062,956 , GRCh38.p12 chr9: 97,428,466-100,300,674 FOXE1, LOC107987011, 47 more genes
    nsv6301951copy number variation1nstd186human GRCh37 chr9: 100,358,470-100,420,655 , GRCh38.p12 chr9: 97,596,188-97,658,373 , NCBP1, 3 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
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