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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5040665inversion1nstd200human GRCh38 chr3: 94,638,746-100,409,115 , GRCh37.p13 chr3: 94,357,590-100,127,959 , LOC101929278, 82 more genes
    nsv5034224inversion1nstd200human GRCh38 chr3: 94,859,289-102,665,887 , GRCh37.p13 chr3: 94,578,133-102,384,731 , LOC105374005, 114 more genes
    nsv4912044copy number variation1nstd200human GRCh38 chr3: 95,148,509-95,180,825 , GRCh37.p13 chr3: 94,867,353-94,899,669 RPS18P6
    nsv4887622inversion1nstd200human GRCh37 chr3: 94,357,590-100,127,961 , GRCh38.p12 chr3: 94,638,746-100,409,117 , CPOX, 82 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4797537copy number variation1nstd200human GRCh37 chr3: 94,867,353-94,899,669 , GRCh38.p12 chr3: 95,148,509-95,180,825 RPS18P6
    nsv4713492copy number variation1nstd195human GRCh37 chr3: 94,784,651-95,001,801 , GRCh38.p12 chr3: 95,065,807-95,282,957 RPS18P6
    nsv4713059copy number variation1nstd195human GRCh37 chr3: 94,784,751-95,001,951 , GRCh38.p12 chr3: 95,065,907-95,283,107 RPS18P6
    nsv4679686copy number variation1nstd189human GRCh37.p13 chr3: 93,519,479-97,386,798 , GRCh38.p12 chr3: 93,800,635-97,667,954 PROS1, NSUN3, 25 more genes
    nsv4674369copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 93,516,594-96,012,342 , GRCh38.p12 chr3: 93,797,750-96,293,498 PROS1, NSUN3, 14 more genes
    nsv4586913copy number variation1nstd183human GRCh37 chr3: 94,785,401-95,181,130 , GRCh38.p12 chr3: 95,066,557-95,462,286 RPS18P6
    nsv4586816copy number variation1nstd183human GRCh37 chr3: 94,882,135-94,911,014 , GRCh38.p12 chr3: 95,163,291-95,192,170 RPS18P6
    nsv4386397copy number variation1nstd173human GRCh37 chr3: 94,820,235-95,012,901 , GRCh38.p12 chr3: 95,101,391-95,294,057 RPS18P6
    nsv4383990copy number variation1nstd173human GRCh37 chr3: 94,890,828-94,917,273 , GRCh38.p12 chr3: 95,171,984-95,198,429 RPS18P6
    nsv4381337copy number variation1nstd173human GRCh37 chr3: 93,809,825-96,377,584 , GRCh38.p12 chr3: 94,090,981-96,658,740 RPS18P6, MIR8060, 11 more genes
    nsv3924517copy number variation1nstd102humanUncertain significance NCBI36 chr3: 95,289,822-97,877,549 , GRCh37.p13 chr3: 93,807,132-96,394,859 , GRCh38.p12 chr3: 94,088,288-96,676,015 HNRNPKP4, RNU6-1094P, 11 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3918661copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683 MTCO2P29, GAP43, 401 more genes
    nsv3917160copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903 ATP6V1A, RPS10P4, 297 more genes
    nsv3911724copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 95,021,157-105,090,283 , GRCh37 chr3: 93,538,467-103,607,593 , GRCh38 chr3: 93,819,623-103,888,749 COL8A1, CPOX, 132 more genes
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