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Items: 1 to 20 of 333

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7061759inversion1nstd229human GRCh38 chr17: 76,882,348-76,882,484 , GRCh37.p13 chr17: 74,878,430-74,878,566 MGAT5B
    nsv6993003copy number variation1nstd229human GRCh38 chr17: 76,933,157-76,970,928 , GRCh37.p13 chr17: 74,929,239-74,967,010 MGAT5B, LOC105371899
    nsv6992633copy number variation1nstd229human GRCh38 chr17: 76,942,348-76,970,726 , GRCh37.p13 chr17: 74,938,430-74,966,808 MGAT5B, LOC105371899
    nsv6990938copy number variation1nstd229human GRCh38 chr17: 76,794,590-76,897,980 , GRCh37.p13 chr17: 74,790,672-74,894,062 LINC02080, MGAT5B, 3 more genes
    nsv6988089copy number variation1nstd229human GRCh38 chr17: 76,873,878-76,878,333 , GRCh37.p13 chr17: 74,869,960-74,874,415 MGAT5B
    nsv6984802copy number variation1nstd229human GRCh38 chr17: 76,867,725-76,922,047 , GRCh37.p13 chr17: 74,863,807-74,918,129 MGAT5B
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6983392copy number variation1nstd229human GRCh38 chr17: 76,896,623-76,899,223 , GRCh37.p13 chr17: 74,892,705-74,895,305 MGAT5B
    nsv6983210copy number variation1nstd229human GRCh38 chr17: 76,897,688-76,897,732 , GRCh37.p13 chr17: 74,893,770-74,893,814 MGAT5B
    nsv6982683copy number variation1nstd229human GRCh38 chr17: 76,908,386-76,913,433 , GRCh37.p13 chr17: 74,904,468-74,909,515 MGAT5B
    nsv6982239copy number variation1nstd229human GRCh38 chr17: 76,224,241-77,998,670 , GRCh37.p13 chr17: 74,220,322-75,994,751 MFSD11, PRPSAP1, 59 more genes
    nsv6981740copy number variation1nstd229human GRCh38 chr17: 76,917,763-76,963,344 , GRCh37.p13 chr17: 74,913,845-74,959,426 LOC105371899, MGAT5B
    nsv6624349copy number variation1nstd224human GRCh37 chr17: 74,870,797-74,916,979 , GRCh38.p12 chr17: 76,874,715-76,920,897 MGAT5B
    nsv6624310copy number variation1nstd224human GRCh37 chr17: 74,878,373-75,004,213 , GRCh38.p12 chr17: 76,882,291-77,008,131 MGAT5B, LOC105371899
    nsv6594840inversion1nstd223human GRCh38 chr17: 76,891,292-76,892,000 , GRCh37.p13 chr17: 74,887,374-74,888,082 MGAT5B
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6534230copy number variation1nstd223human GRCh38 chr17: 76,931,687-76,932,579 , GRCh37.p13 chr17: 74,927,769-74,928,661 MGAT5B
    nsv6530843copy number variation1nstd223human GRCh38 chr17: 76,735,301-77,145,300 , GRCh37.p13 chr17: 74,731,383-75,141,382 SEC14L1, RNU6-97P, 12 more genes
    nsv6529279copy number variation1nstd223human GRCh38 chr17: 76,916,964-76,917,485 , GRCh37.p13 chr17: 74,913,046-74,913,567 MGAT5B
    nsv6528773copy number variation1nstd223human GRCh38 chr17: 76,913,701-76,914,700 , GRCh37.p13 chr17: 74,909,783-74,910,782 MGAT5B
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