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Items: 1 to 20 of 312

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077794inversion1nstd229human GRCh38 chr9: 6,332,340-8,931,710 , GRCh37.p13 chr9: 6,332,340-8,931,710 PRELID3BP11, UHRF2, 22 more genes
    nsv7071360inversion1nstd229human GRCh38 chr9: 6,372,642-8,080,498 , GRCh37.p13 chr9: 6,372,642-8,080,498 PPIAP33, GLDC, 17 more genes
    nsv7069216inversion1nstd229human GRCh38 chr9: 7,791,759-7,931,967 , GRCh37.p13 chr9: 7,791,759-7,931,967 LOC105375971, DMAC1
    nsv7066230inversion1nstd229human GRCh38 chr9: 235,930-9,843,002 , GRCh37.p13 chr9: 235,930-9,843,002 GLIS3-AS1, LOC105375955, 118 more genes
    nsv7061351inversion1nstd229human GRCh38 chr9: 6,221,482-9,809,904 , GRCh37.p13 chr9: 6,221,482-9,809,904 LOC105375969, LOC105375972, 28 more genes
    nsv6874536copy number variation1nstd229human GRCh38 chr9: 7,651,021-7,994,124 , GRCh37.p13 chr9: 7,651,021-7,994,124 LOC105375971, DMAC1
    nsv6864242copy number variation1nstd229human GRCh38 chr9: 7,796,842-7,796,869 , GRCh37.p13 chr9: 7,796,842-7,796,869 DMAC1
    nsv6860958copy number variation1nstd229human GRCh38 chr9: 7,578,110-8,162,648 , GRCh37.p13 chr9: 7,578,110-8,162,648 PPIAP33, LOC105375971, 1 more genes
    nsv6860421copy number variation1nstd229human GRCh38 chr9: 5,097,512-15,003,390 , GRCh37.p13 chr9: 5,097,512-15,003,388 LOC102724027, ATP5PDP3, 89 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
    nsv6634450copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-15,048,247 , GRCh38.p12 chr9: 203,861-15,048,249 LOC102724027, DMRT2, 157 more genes
    nsv6634421copy number variation1nstd102humanPathogenic GRCh37 chr9: 6,825,346-10,816,593 , GRCh38.p12 chr9: 6,825,346-10,816,593 PPIAP33, LOC105375971, 15 more genes
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6633476copy number variation1nstd224human GRCh37 chr9: 7,560,568-7,874,458 , GRCh38.p12 chr9: 7,560,568-7,874,458 PPIAP33, DMAC1
    nsv6573936inversion1nstd223human GRCh38 chr9: 6,372,642-8,080,498 , GRCh37.p13 chr9: 6,372,642-8,080,498 PRELID3BP11, UHRF2, 17 more genes
    nsv6426248copy number variation1nstd223human GRCh38 chr9: 6,136,627-9,932,176 , GRCh37.p13 chr9: 6,136,627-9,932,176 RPS26P3, KDM4C, 29 more genes
    nsv6315522copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-10,283,912 , GRCh38.p12 chr9: 203,861-10,283,912 DMAC1, RNU7-185P, 119 more genes
    nsv6315463copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-35,903,398 , GRCh38.p12 chr9: 203,861-35,903,401 IFNA11P, RNU6-14P, 495 more genes
    nsv6315458copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-12,570,076 , GRCh38.p12 chr9: 203,861-12,570,076 LINC02851, GLIS3, 129 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
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