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Items: 15

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    Number of Variants: 15

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3317857copy number variation22nstd157human GRCh37 chr15: 56,789,979-56,800,635 , GRCh38.p12 chr15: 56,497,781-56,508,437
    nsv3318265copy number variation3nstd157human GRCh37 chr2: 228,243,310-228,258,198 , GRCh38.p12 chr2: 227,378,594-227,393,482 TM4SF20
    nsv3318251copy number variation25nstd157human GRCh38.p12 chr12: 2,136,470-2,145,053 , GRCh37 chr12: 2,245,636-2,254,219 , GRCh38.p12 chr12|NW_018654718.1: 478,614-487,197 CACNA1C, LOC107984131
    nsv3317548copy number variation1nstd157human GRCh38.p12 chr1: 1,716,247-1,732,685 , GRCh37 chr1: 1,647,686-1,664,124 SLC35E2A, CDK11A
    nsv3318220copy number variation21nstd157human GRCh38.p12 chr19: 20,418,529-20,532,427 , GRCh37 chr19: 20,601,335-20,715,233 ZNF826P, ZNF737, 3 more genes
    nsv3317392copy number variation23nstd157human GRCh38.p12 chr4: 68,527,638-68,623,755 , GRCh37 chr4: 69,393,356-69,489,473 UGT2B17, LOC100132651, 1 more genes
    nsv3318874copy number variation4nstd157human GRCh38.p12 chr16: 75,505,538-75,544,521 , GRCh37 chr16: 75,539,436-75,578,419 CHST5, TMEM231, 1 more genes
    nsv3318172copy number variation11nstd157human GRCh37 chr14: 86,285,493-86,312,888 , GRCh38.p12 chr14: 85,819,149-85,846,544 0
    nsv3317859copy number variation29nstd157human GRCh37 chr4: 64,136,609-64,154,477 , GRCh38.p12 chr4: 63,270,891-63,288,759 0
    nsv3318308copy number variation19nstd157human GRCh37 chr16: 19,945,540-19,962,636 , GRCh38.p12 chr16: 19,934,218-19,951,314 0
    nsv3317289copy number variation24nstd157human GRCh37 chr9: 24,502,737-24,518,795 , GRCh38.p12 chr9: 24,502,739-24,518,797 0
    nsv3317224copy number variation21nstd157human GRCh37 chr10: 82,879,475-82,891,283 , GRCh38.p12 chr10: 81,119,719-81,131,527 0
    nsv3318432copy number variation41nstd157human GRCh37 chr8: 5,595,511-5,605,706 , GRCh38.p12 chr8: 5,737,989-5,748,184 0
    nsv3318230copy number variation25nstd157human GRCh37 chr2: 184,795,725-184,803,456 , GRCh38.p12 chr2: 183,930,998-183,938,729 0
    nsv3317294copy number variation14nstd157human GRCh38.p12 chr4: 59,114,344-59,122,377 , GRCh37 chr4: 59,980,062-59,988,095 0
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