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Items: 1 to 20 of 201

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122866copy number variation1nstd186human GRCh37 chr11: 118,418,487-118,419,315 , GRCh38.p12 chr11: 118,547,772-118,548,600 IFT46
    nsv5914384copy number variation1nstd209human GRCh38 chr11: 118,537,152-118,551,182 , GRCh37.p13 chr11|NW_003871072.2: 162,590-176,620 , GRCh37.p13 chr11: 118,407,867-118,421,897 IFT46, TMEM25
    nsv5914008copy number variation1nstd209human GRCh38 chr11: 118,547,983-118,548,599 , GRCh37.p13 chr11: 118,418,698-118,419,314 , GRCh37.p13 chr11|NW_003871072.2: 173,421-174,037 IFT46
    nsv5911397copy number variation1nstd209human GRCh38 chr11: 118,549,672-118,549,740 , GRCh37.p13 chr11|NW_003871072.2: 175,110-175,178 , GRCh37.p13 chr11: 118,420,387-118,420,455 IFT46
    nsv5910798copy number variation1nstd209human GRCh38 chr11: 118,566,475-118,567,358 , GRCh37.p13 chr11|NW_003871072.2: 191,913-192,796 , GRCh37.p13 chr11: 118,437,190-118,438,073 IFT46
    nsv5866395copy number variation1nstd209human GRCh38 chr11: 118,537,125-118,543,124 , GRCh37.p13 chr11|NW_003871072.2: 162,563-168,562 , GRCh37.p13 chr11: 118,407,840-118,413,839 TMEM25, IFT46
    nsv5513319copy number variation1nstd206human GRCh38 chr11: 118,563,040-118,564,101 , GRCh37.p13 chr11: 118,433,755-118,434,816 , GRCh37.p13 chr11|NW_003871072.2: 188,478-189,539 IFT46
    nsv5505661copy number variation1nstd206human GRCh38 chr11: 118,542,776-118,542,906 , GRCh37.p13 chr11|NW_003871072.2: 168,214-168,344 , GRCh37.p13 chr11: 118,413,491-118,413,621 IFT46, TMEM25
    nsv5503237copy number variation1nstd206human GRCh38 chr11: 118,547,772-118,548,600 , GRCh37.p13 chr11|NW_003871072.2: 173,210-174,038 , GRCh37.p13 chr11: 118,418,487-118,419,315 IFT46
    nsv5502209copy number variation1nstd206human GRCh38 chr11: 118,502,169-118,560,697 , GRCh37.p13 chr11|NW_003871072.2: 127,607-186,135 , GRCh37.p13 chr11: 118,372,884-118,431,412 KMT2A, IFT46, 4 more genes
    nsv5494546copy number variation1nstd206human GRCh38 chr11: 118,541,193-118,543,033 , GRCh37.p13 chr11: 118,411,908-118,413,748 , GRCh37.p13 chr11|NW_003871072.2: 166,631-168,471 TMEM25, IFT46
    nsv5392548copy number variation1nstd186human GRCh37 chr11: 118,418,874-118,419,324 , GRCh38.p12 chr11: 118,548,159-118,548,609 IFT46
    nsv5391764copy number variation1nstd186human GRCh37 chr11: 118,418,737-118,419,259 , GRCh38.p12 chr11: 118,548,022-118,548,544 IFT46
    nsv5320184copy number variation1nstd204human GRCh37.p13 chr11|NW_003871072.2: 127,606-186,136 , GRCh37.p13 chr11: 118,372,883-118,431,413 , GRCh38.p13 chr11: 118,502,168-118,560,698 KMT2A, IFT46, 4 more genes
    nsv5304059copy number variation1nstd204human GRCh38.p13 chr11: 118,547,982-118,548,582 , GRCh37.p13 chr11|NW_003871072.2: 173,420-174,020 , GRCh37.p13 chr11: 118,418,697-118,419,297 IFT46
    nsv5278001copy number variation1nstd204human GRCh38.p13 chr11: 118,558,201-118,561,158 , GRCh37.p13 chr11|NW_003871072.2: 183,639-186,596 , GRCh37.p13 chr11: 118,428,916-118,431,873 RPL5P30, IFT46
    nsv5275564copy number variation1nstd204human GRCh38.p13 chr11: 118,544,375-118,546,674 , GRCh37.p13 chr11|NW_003871072.2: 169,813-172,112 , GRCh37.p13 chr11: 118,415,090-118,417,389 IFT46, TMEM25
    nsv5274704copy number variation1nstd204human GRCh38.p13 chr11: 118,502,101-118,558,400 , GRCh37.p13 chr11: 118,372,816-118,429,115 , GRCh37.p13 chr11|NW_003871072.2: 127,539-183,838 KMT2A, IFT46, 3 more genes
    nsv5273685copy number variation1nstd204human GRCh38.p13 chr11: 118,540,301-118,558,700 , GRCh37.p13 chr11: 118,411,016-118,429,415 , GRCh37.p13 chr11|NW_003871072.2: 165,739-184,138 IFT46, RPL5P30, 1 more genes
    nsv5271274copy number variation1nstd204human GRCh38.p13 chr11: 118,500,999-118,544,224 , GRCh37.p13 chr11|NW_003871072.2: 126,437-169,662 , GRCh37.p13 chr11: 118,371,714-118,414,939 KMT2A, IFT46, 3 more genes
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