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Items: 1 to 20 of 1191

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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
    nsv7074632inversion1nstd229human GRCh38 chr18: 36,557,558-36,557,585 , GRCh37.p13 chr18: 34,137,521-34,137,548 FHOD3
    nsv7071883inversion1nstd229human GRCh38 chr18: 36,524,006-36,526,696 , GRCh37.p13 chr18: 34,103,969-34,106,659 FHOD3
    nsv7071414inversion1nstd229human GRCh38 chr18: 36,604,708-36,604,768 , GRCh37.p13 chr18: 34,184,671-34,184,731 FHOD3
    nsv7058254inversion1nstd229human GRCh38 chr18: 36,591,094-36,839,834 , GRCh37.p13 chr18: 34,171,057-34,419,797 KIAA1328, TPGS2, 2 more genes
    nsv7017885copy number variation1nstd229human GRCh38 chr18: 36,673,110-36,679,900 , GRCh37.p13 chr18: 34,253,073-34,259,863 FHOD3
    nsv7017513copy number variation1nstd229human GRCh38 chr18: 36,335,598-36,802,582 , GRCh37.p13 chr18: 33,915,561-34,382,545 FHOD3, LOC105372071, 1 more genes
    nsv7017097copy number variation1nstd229human GRCh38 chr18: 36,480,897-36,481,125 , GRCh37.p13 chr18: 34,060,860-34,061,088 FHOD3
    nsv7016720copy number variation1nstd229human GRCh38 chr18: 36,536,440-36,539,281 , GRCh37.p13 chr18: 34,116,403-34,119,244 FHOD3
    nsv7016485copy number variation1nstd229human GRCh38 chr18: 36,330,217-36,330,352 , GRCh37.p13 chr18: 33,910,180-33,910,315 FHOD3
    nsv7016480copy number variation1nstd229human GRCh38 chr18: 36,764,901-36,772,500 , GRCh37.p13 chr18: 34,344,864-34,352,463 FHOD3
    nsv7015707copy number variation1nstd229human GRCh38 chr18: 36,337,216-36,345,446 , GRCh37.p13 chr18: 33,917,179-33,925,409 FHOD3
    nsv7015583copy number variation1nstd229human GRCh38 chr18: 36,353,898-36,353,986 , GRCh37.p13 chr18: 33,933,861-33,933,949 FHOD3
    nsv7015491copy number variation1nstd229human GRCh38 chr18: 36,746,917-36,747,130 , GRCh37.p13 chr18: 34,326,880-34,327,093 FHOD3
    nsv7014669copy number variation1nstd229human GRCh38 chr18: 36,350,031-36,356,913 , GRCh37.p13 chr18: 33,929,994-33,936,876 FHOD3
    nsv7014668copy number variation1nstd229human GRCh38 chr18: 36,470,871-36,471,542 , GRCh37.p13 chr18: 34,050,834-34,051,505 FHOD3
    nsv7013809copy number variation1nstd229human GRCh38 chr18: 36,301,501-36,307,144 , GRCh37.p13 chr18: 33,881,464-33,887,107 FHOD3
    nsv7013760copy number variation1nstd229human GRCh38 chr18: 36,734,973-36,735,513 , GRCh37.p13 chr18: 34,314,936-34,315,476 FHOD3
    nsv7013727copy number variation1nstd229human GRCh38 chr18: 36,373,601-36,394,800 , GRCh37.p13 chr18: 33,953,564-33,974,763 FHOD3
    nsv7013629copy number variation1nstd229human GRCh38 chr18: 36,318,798-36,323,151 , GRCh37.p13 chr18: 33,898,761-33,903,114 FHOD3
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