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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062534inversion1nstd229human GRCh38 chr11: 83,132,580-86,771,462 , GRCh37.p13 chr11: 82,843,622-86,482,504 CCDC83, LOC100421303, 44 more genes
    nsv6918009copy number variation1nstd229human GRCh38 chr11: 83,261,739-83,346,263 , GRCh37.p13 chr11: 82,972,781-83,057,306 LOC105369420, CYCSP28, 1 more genes
    nsv6915527copy number variation1nstd229human GRCh38 chr11: 82,974,601-83,470,600 , GRCh37.p13 chr11: 82,685,643-83,181,643 CYCSP28, DLG2, 14 more genes
    nsv6914805copy number variation1nstd229human GRCh38 chr11: 83,282,458-83,285,090 , GRCh37.p13 chr11: 82,993,501-82,996,133 CCDC90B
    nsv6906278copy number variation1nstd229human GRCh38 chr11: 83,255,554-83,349,247 , GRCh37.p13 chr11: 82,966,596-83,060,290 LOC105369420, CCDC90B, 2 more genes
    nsv6903014copy number variation1nstd229human GRCh38 chr11: 83,237,179-83,261,561 , GRCh37.p13 chr11: 82,948,221-82,972,603 CCDC90B, ANKRD42
    nsv6902459copy number variation1nstd229human GRCh38 chr11: 83,258,113-83,342,023 , GRCh37.p13 chr11: 82,969,155-83,053,066 CCDC90B, CYCSP28, 1 more genes
    nsv6899904copy number variation1nstd229human GRCh38 chr11: 83,254,452-83,273,276 , GRCh37.p13 chr11: 82,965,494-82,984,319 ANKRD42, CCDC90B
    nsv6637847copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,562,738-88,663,067 , GRCh38.p12 chr11: 80,851,695-88,929,899 PRSS23, MTCO3P25, 92 more genes
    nsv6637436copy number variation1nstd102humanUncertain significance GRCh37 chr11: 82,964,288-83,060,768 , GRCh38.p12 chr11: 83,253,246-83,349,725 CCDC90B, LOC105369420, 2 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6637282copy number variation1nstd102humanUncertain significance GRCh37 chr11: 82,859,094-83,324,406 , GRCh38.p12 chr11: 83,148,052-83,613,363 CKS1BP4, ANKRD42, 9 more genes
    nsv6621270copy number variation1nstd224human GRCh37 chr11: 82,972,960-83,041,907 , GRCh38.p12 chr11: 83,261,918-83,330,864 LOC105369420, CCDC90B, 1 more genes
    nsv6472257copy number variation1nstd223human GRCh38 chr11: 83,254,462-83,273,248 , GRCh37.p13 chr11: 82,965,504-82,984,291 ANKRD42, CCDC90B
    nsv6466654copy number variation1nstd223human GRCh38 chr11: 83,275,284-83,275,840 , GRCh37.p13 chr11: 82,986,327-82,986,883 CCDC90B
    nsv6464848copy number variation1nstd223human GRCh38 chr11: 83,269,495-83,271,656 , GRCh37.p13 chr11: 82,980,537-82,982,698 CCDC90B
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6313961copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717 MTND5P38, XIAPP2, 252 more genes
    nsv6132285copy number variation1nstd213human GRCh37 chr11: 82,730,000-83,280,001 , GRCh38.p12 chr11: 83,018,958-83,568,958 DLG2, PCF11, 15 more genes
    nsv5923590copy number variation1nstd209human GRCh38 chr11: 83,256,823-83,268,098 , GRCh37.p13 chr11: 82,967,865-82,979,140 CCDC90B
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