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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923389copy number variation1nstd209human GRCh38 chr7: 107,680,049-107,680,135 , GRCh37.p13 chr7: 107,320,494-107,320,580 SLC26A4
    nsv5673927copy number variation1nstd102humanPathogenic GRCh37 chr7: 107,301,201-107,324,012 , GRCh38.p12 chr7: 107,660,756-107,683,567 SLC26A4-AS1, SLC26A4
    nsv5673784copy number variation1nstd102humanPathogenic GRCh37 chr7: 107,303,728-107,303,890 , GRCh38.p12 chr7: 107,663,283-107,663,445 SLC26A4
    nsv5673609copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 107,336,368-107,355,960 , GRCh38.p12 chr7: 107,695,923-107,715,515 SLC26A4
    nsv5642798insertion1nstd207human GRCh38 chr7: 107,686,290-107,686,290 , GRCh37.p13 chr7: 107,326,735-107,326,735 SLC26A4
    nsv5627351insertion1nstd207human GRCh38 chr7: 107,679,869-107,679,869 , GRCh37.p13 chr7: 107,320,314-107,320,314 SLC26A4
    nsv5573793copy number variation1nstd207human GRCh38 chr7: 107,680,063-107,680,177 , GRCh37.p13 chr7: 107,320,508-107,320,622 SLC26A4
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5493390copy number variation1nstd206human GRCh38 chr7: 107,714,228-107,715,721 , GRCh37.p13 chr7: 107,354,673-107,356,166 SLC26A4
    nsv5486581copy number variation1nstd206human GRCh38 chr7: 107,567,980-107,665,961 , GRCh37.p13 chr7: 107,208,425-107,306,406 , SLC26A4, 6 more genes
    nsv5483389copy number variation1nstd206human GRCh38 chr7: 107,712,742-107,714,257 , GRCh37.p13 chr7: 107,353,187-107,354,702 SLC26A4
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4950715copy number variation1nstd200human GRCh38 chr7: 107,717,320-107,718,841 , GRCh37.p13 chr7: 107,357,765-107,359,286 SLC26A4
    nsv4950714copy number variation1nstd200human GRCh38 chr7: 107,661,479-107,663,854 , GRCh37.p13 chr7: 107,301,924-107,304,299 SLC26A4, SLC26A4-AS1
    nsv4893211mobile element deletion1nstd200human GRCh38 chr7: 107,675,563-107,675,873 , GRCh37.p13 chr7: 107,316,008-107,316,318 SLC26A4
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4819946copy number variation1nstd200human GRCh37 chr7: 107,353,218-107,355,838 , GRCh38.p12 chr7: 107,712,773-107,715,393 SLC26A4
    nsv4819945copy number variation1nstd200human GRCh37 chr7: 107,301,924-107,304,299 , GRCh38.p12 chr7: 107,661,479-107,663,854 SLC26A4, SLC26A4-AS1
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