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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4983879copy number variation1nstd200human GRCh38 chr10: 25,046,588-25,104,327 , GRCh37.p13 chr10: 25,335,517-25,393,256 ENKUR
    nsv4975462copy number variation1nstd200human GRCh38 chr10: 24,969,109-24,980,941 , GRCh37.p13 chr10: 25,258,038-25,269,870 ENKUR, THNSL1
    nsv4899504mobile element deletion1nstd200human GRCh38 chr10: 25,058,649-25,058,944 , GRCh37.p13 chr10: 25,347,578-25,347,873 ENKUR
    nsv4829575copy number variation1nstd200human GRCh37 chr10: 25,335,517-25,393,256 , GRCh38.p12 chr10: 25,046,588-25,104,327 ENKUR
    nsv4785850mobile element deletion1nstd200human GRCh37 chr10: 25,347,578-25,347,873 , GRCh38.p12 chr10: 25,058,649-25,058,944 ENKUR
    nsv4735959copy number variation1nstd199human GRCh37 chr10: 25,277,591-25,277,643 , GRCh38.p12 chr10: 24,988,662-24,988,714 THNSL1, ENKUR
    nsv4730449copy number variation1nstd199human GRCh37 chr10: 25,347,618-25,347,687 , GRCh38.p12 chr10: 25,058,689-25,058,758 ENKUR
    nsv4680146copy number variation1nstd189human GRCh37.p13 chr10: 25,323,164-25,627,827 , GRCh38.p12 chr10: 25,034,235-25,338,898 GPR158, ENKUR, 2 more genes
    nsv4611536copy number variation1nstd183human GRCh37 chr10: 25,337,604-25,377,933 , GRCh38.p12 chr10: 25,048,675-25,089,004 ENKUR
    nsv4577700mobile element insertion1nstd166human GRCh37.p13 chr10: 25,330,601-25,330,601 , GRCh38.p12 chr10: 25,041,672-25,041,672 ENKUR
    nsv4565315mobile element insertion1nstd166human GRCh37.p13 chr10: 25,336,686-25,336,686 , GRCh38.p12 chr10: 25,047,757-25,047,757 ENKUR
    nsv4455901copy number variation1nstd102humanUncertain significance GRCh37 chr10: 25,133,682-25,277,446 , GRCh38.p12 chr10: 24,844,753-24,988,517 THNSL1, ENKUR, 2 more genes
    nsv4418398copy number variation1nstd174human GRCh37 chr10: 25,277,423-25,277,846 , GRCh38.p12 chr10: 24,988,494-24,988,917 ENKUR, THNSL1
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4190588copy number variation1nstd166human GRCh37.p13 chr10: 25,341,900-25,343,138 , GRCh38.p12 chr10: 25,052,971-25,054,209 ENKUR
    nsv4182275copy number variation1nstd166human GRCh37.p13 chr10: 25,304,162-25,307,763 , GRCh38.p12 chr10: 25,015,233-25,018,834 THNSL1, ENKUR
    nsv4180298copy number variation1nstd166human GRCh37.p13 chr10: 25,347,923-25,353,703 , GRCh38.p12 chr10: 25,058,994-25,064,774 ENKUR
    nsv4173908copy number variation1nstd166human GRCh37.p13 chr10: 25,258,069-25,269,841 , GRCh38.p12 chr10: 24,969,140-24,980,912 THNSL1, ENKUR
    nsv3933467copy number variation1nstd167human GRCh37 chr10: 25,277,593-25,277,641 , GRCh38.p12 chr10: 24,988,664-24,988,712 THNSL1, ENKUR
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 EPC1-AS1, RNU6-452P, 559 more genes
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