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Items: 1 to 20 of 814

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076342inversion1nstd229human GRCh38 chr18: 36,552,732-40,928,121 , GRCh37.p13 chr18: 34,132,695-38,508,085 CELF4, LOC105372074, 32 more genes
    nsv7018069copy number variation1nstd229human GRCh38 chr18: 37,373,318-37,377,942 , GRCh37.p13 chr18: 34,953,281-34,957,905 CELF4
    nsv7016042copy number variation1nstd229human GRCh38 chr18: 37,522,904-37,536,786 , GRCh37.p13 chr18: 35,102,867-35,116,749 CELF4
    nsv7015030copy number variation1nstd229human GRCh38 chr18: 37,131,926-37,307,439 , GRCh37.p13 chr18: 34,711,889-34,887,402 LOC105372068, KIAA1328, 1 more genes
    nsv7014585copy number variation1nstd229human GRCh38 chr18: 37,411,594-37,414,841 , GRCh37.p13 chr18: 34,991,557-34,994,804 CELF4
    nsv7014468copy number variation1nstd229human GRCh38 chr18: 37,355,101-37,357,400 , GRCh37.p13 chr18: 34,935,064-34,937,363 CELF4
    nsv7014448copy number variation1nstd229human GRCh38 chr18: 37,301,035-37,306,910 , GRCh37.p13 chr18: 34,880,998-34,886,873 CELF4
    nsv7013020copy number variation1nstd229human GRCh38 chr18: 37,521,591-37,521,797 , GRCh37.p13 chr18: 35,101,554-35,101,760 CELF4
    nsv7012473copy number variation1nstd229human GRCh38 chr18: 37,411,592-37,414,840 , GRCh37.p13 chr18: 34,991,555-34,994,803 CELF4
    nsv7011826copy number variation1nstd229human GRCh38 chr18: 37,505,114-37,505,149 , GRCh37.p13 chr18: 35,085,077-35,085,112 CELF4
    nsv7011816copy number variation1nstd229human GRCh38 chr18: 37,276,466-37,290,071 , GRCh37.p13 chr18: 34,856,429-34,870,034 CELF4, LOC105372068
    nsv7011109copy number variation1nstd229human GRCh38 chr18: 37,337,254-37,340,406 , GRCh37.p13 chr18: 34,917,217-34,920,369 CELF4
    nsv7011018copy number variation1nstd229human GRCh38 chr18: 37,282,005-37,284,519 , GRCh37.p13 chr18: 34,861,968-34,864,482 CELF4
    nsv7010335copy number variation1nstd229human GRCh38 chr18: 37,499,930-37,509,893 , GRCh37.p13 chr18: 35,079,893-35,089,856 CELF4
    nsv7010274copy number variation1nstd229human GRCh38 chr18: 37,408,501-37,458,200 , GRCh37.p13 chr18: 34,988,464-35,038,163 CELF4
    nsv7008323copy number variation1nstd229human GRCh38 chr18: 37,459,201-37,464,000 , GRCh37.p13 chr18: 35,039,164-35,043,963 CELF4
    nsv7007720copy number variation1nstd229human GRCh38 chr18: 37,405,441-37,427,253 , GRCh37.p13 chr18: 34,985,404-35,007,216 CELF4
    nsv7007438copy number variation1nstd229human GRCh38 chr18: 37,409,503-37,417,891 , GRCh37.p13 chr18: 34,989,466-34,997,854 CELF4
    nsv7007281copy number variation1nstd229human GRCh38 chr18: 37,233,009-37,274,088 , GRCh37.p13 chr18: 34,812,972-34,854,051 LOC105372068, CELF4
    nsv7006954copy number variation1nstd229human GRCh38 chr18: 37,233,031-37,397,072 , GRCh37.p13 chr18: 34,812,994-34,977,035 CELF4, LOC105372068
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