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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099193copy number variation1nstd231human GRCh38.p12 chr1: 32,456,017-38,905,781 , GRCh37 chr1: 32,921,618-39,371,453 AK2, COL8A2, 151 more genes
    nsv7046918inversion1nstd229human GRCh38 chr1: 34,689,928-38,980,899 , GRCh37.p13 chr1: 35,155,529-39,446,571 LOC105378647, NCDN, 112 more genes
    nsv6649833copy number variation1nstd229human GRCh38 chr1: 38,929,909-38,942,329 , GRCh37.p13 chr1: 39,395,581-39,408,001 RHBDL2
    nsv6649114copy number variation1nstd229human GRCh38 chr1: 38,935,994-38,938,882 , GRCh37.p13 chr1: 39,401,666-39,404,554 RHBDL2
    nsv6649113copy number variation1nstd229human GRCh38 chr1: 38,928,589-38,931,952 , GRCh37.p13 chr1: 39,394,261-39,397,624 RHBDL2
    nsv6649112copy number variation1nstd229human GRCh38 chr1: 38,921,160-38,925,249 , GRCh37.p13 chr1: 39,386,832-39,390,921 RHBDL2, RNU6-605P
    nsv6649111copy number variation1nstd229human GRCh38 chr1: 38,890,239-38,894,909 , GRCh37.p13 chr1: 39,355,911-39,360,581 RHBDL2
    nsv6626377copy number variation1nstd224human GRCh37 chr1: 39,350,742-39,361,681 , GRCh38.p12 chr1: 38,885,070-38,896,009 RHBDL2
    nsv6551942inversion1nstd223human GRCh38 chr1: 38,901,700-38,902,671 , GRCh37.p13 chr1: 39,367,372-39,368,343 RHBDL2
    nsv6546825inversion1nstd223human GRCh38 chr1: 38,901,278-38,902,447 , GRCh37.p13 chr1: 39,366,950-39,368,119 RHBDL2
    nsv6545099inversion1nstd223human GRCh38 chr1: 38,924,901-38,925,023 , GRCh37.p13 chr1: 39,390,573-39,390,695 RNU6-605P, RHBDL2
    nsv6334181copy number variation1nstd223human GRCh38 chr1: 38,883,914-38,884,557 , GRCh37.p13 chr1: 39,349,586-39,350,229 RHBDL2
    nsv6333387copy number variation1nstd223human GRCh38 chr1: 38,926,560-38,927,150 , GRCh37.p13 chr1: 39,392,232-39,392,822 RNU6-605P, RHBDL2
    nsv6328123copy number variation1nstd223human GRCh38 chr1: 38,919,825-38,920,419 , GRCh37.p13 chr1: 39,385,497-39,386,091 RHBDL2, LOC105378662
    nsv6319129copy number variation1nstd223human GRCh38 chr1: 38,929,908-38,942,328 , GRCh37.p13 chr1: 39,395,580-39,408,000 RHBDL2
    nsv6318600copy number variation1nstd223human GRCh38 chr1: 38,904,228-38,913,955 , GRCh37.p13 chr1: 39,369,900-39,379,627 RHBDL2, LOC105378662
    nsv6317333copy number variation1nstd223human GRCh38 chr1: 38,919,775-38,937,115 , GRCh37.p13 chr1: 39,385,447-39,402,787 RNU6-605P, RHBDL2, 1 more genes
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
    nsv6313549copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 38,679,545-42,556,292 , GRCh38.p12 chr1: 38,213,873-42,090,621 BMP8B, COL9A2, 93 more genes
    nsv6299209copy number variation1nstd186human GRCh37 chr1: 39,401,666-39,404,551 , GRCh38.p12 chr1: 38,935,994-38,938,879 RHBDL2
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