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Items: 1 to 20 of 427

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7069364inversion1nstd229human GRCh38 chr9: 71,375,217-71,711,650 , GRCh37.p13 chr9: 73,990,133-74,326,566 TRPM3, CEMIP2, 1 more genes
    nsv7065303inversion1nstd229human GRCh38 chr9: 71,473,712-72,923,816 , GRCh37.p13 chr9: 74,088,628-75,538,732 LOC101927234, GDA, 21 more genes
    nsv6877923copy number variation1nstd229human GRCh38 chr9: 71,760,405-71,760,702 , GRCh37.p13 chr9: 74,375,321-74,375,618 CEMIP2
    nsv6877003copy number variation1nstd229human GRCh38 chr9: 71,760,412-71,760,703 , GRCh37.p13 chr9: 74,375,328-74,375,619 CEMIP2
    nsv6876187copy number variation1nstd229human GRCh38 chr9: 71,766,800-71,767,169 , GRCh37.p13 chr9: 74,381,716-74,382,085 CEMIP2
    nsv6874706copy number variation1nstd229human GRCh38 chr9: 71,765,072-71,765,279 , GRCh37.p13 chr9: 74,379,988-74,380,195 CEMIP2
    nsv6869513copy number variation1nstd229human GRCh38 chr9: 71,401,871-71,702,485 , GRCh37.p13 chr9: 74,016,787-74,317,401 TRPM3, RPL35AP21, 1 more genes
    nsv6868647copy number variation1nstd229human GRCh38 chr9: 71,736,410-71,829,653 , GRCh37.p13 chr9: 74,351,326-74,444,569 CEMIP2, LOC100420790
    nsv6868585copy number variation1nstd229human GRCh38 chr9: 71,101,404-71,757,322 , GRCh37.p13 chr9: 73,716,320-74,372,238 LOC107987079, TRPM3, 2 more genes
    nsv6868070copy number variation1nstd229human GRCh38 chr9: 71,763,810-71,981,442 , GRCh37.p13 chr9: 74,378,726-74,596,358 LOC100420790, C9orf85, 2 more genes
    nsv6867537copy number variation1nstd229human GRCh38 chr9: 71,726,198-71,728,303 , GRCh37.p13 chr9: 74,341,114-74,343,219 CEMIP2
    nsv6864931copy number variation1nstd229human GRCh38 chr9: 71,206,261-71,879,773 , GRCh37.p13 chr9: 73,821,177-74,494,689 TRPM3, LOC107987079, 4 more genes
    nsv6863733copy number variation1nstd229human GRCh38 chr9: 71,750,177-71,750,267 , GRCh37.p13 chr9: 74,365,093-74,365,183 CEMIP2
    nsv6863179copy number variation1nstd229human GRCh38 chr9: 71,706,079-71,706,849 , GRCh37.p13 chr9: 74,320,995-74,321,765 CEMIP2
    nsv6637502copy number variation1nstd102humanUncertain significance GRCh37 chr9: 70,966,262-76,901,382 , GRCh38.p12 chr9: 68,351,346-74,286,466 RPS20P24, MAMDC2-AS1, 77 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
    nsv6633475copy number variation1nstd224human GRCh37 chr9: 74,363,668-74,454,642 , GRCh38.p12 chr9: 71,748,752-71,839,726 LOC100420790, CEMIP2
    nsv6633474copy number variation1nstd224human GRCh37 chr9: 73,736,227-74,365,261 , GRCh38.p12 chr9: 71,121,311-71,750,345 CEMIP2, LOC107987079, 2 more genes
    nsv6570259inversion1nstd223human GRCh38 chr9: 71,706,003-71,706,991 , GRCh37.p13 chr9: 74,320,919-74,321,907 CEMIP2
    nsv6563970inversion1nstd223human GRCh38 chr9: 71,164,626-72,130,108 , GRCh37.p13 chr9: 73,779,542-74,745,024 ABHD17B, C9orf57, 10 more genes
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