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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5691352mobile element insertion2nstd211human GRCh38 chr7: 123,511,688-123,511,688 , GRCh37.p13 chr7: 123,151,742-123,151,742 IQUB
    nsv5681849mobile element insertion1nstd211human GRCh38 chr7: 123,474,588-123,474,588 , GRCh37.p13 chr7: 123,114,642-123,114,642 IQUB
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5481548copy number variation1nstd206human GRCh38 chr7: 123,483,853-123,486,113 , GRCh37.p13 chr7: 123,123,907-123,126,167 IQUB
    nsv5407027mobile element insertion1nstd206human GRCh38 chr7: 123,511,688-123,511,739 , GRCh37.p13 chr7: 123,151,742-123,151,793 IQUB
    nsv5397806mobile element insertion1nstd206human GRCh38 chr7: 123,474,588-123,474,639 , GRCh37.p13 chr7: 123,114,642-123,114,693 IQUB
    nsv5381759copy number variation1nstd102humanPathogenic GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640 TMEM229A, ST7-OT3, 110 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5195631mobile element insertion1nstd203human GRCh38 chr7: 123,455,108-123,455,118 , GRCh37.p13 chr7: 123,095,162-123,095,172 IQUB
    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
    nsv4968689copy number variation1nstd200human GRCh38 chr7: 123,513,753-123,628,517 , GRCh37.p13 chr7: 123,153,807-123,268,571 ASB15, IQUB, 2 more genes
    nsv4968687copy number variation1nstd200human GRCh38 chr7: 123,313,906-124,175,429 , GRCh37.p13 chr7: 122,953,960-123,815,483 RNU6-11P, TMEM229A, 11 more genes
    nsv4958044copy number variation1nstd200human GRCh38 chr7: 123,524,010-123,532,486 , GRCh37.p13 chr7: 123,164,064-123,172,540 IQUB
    nsv4958043copy number variation1nstd200human GRCh38 chr7: 123,483,853-123,486,113 , GRCh37.p13 chr7: 123,123,907-123,126,167 IQUB
    nsv4958042copy number variation1nstd200human GRCh38 chr7: 123,479,322-123,481,571 , GRCh37.p13 chr7: 123,119,376-123,121,625 IQUB
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4825312copy number variation1nstd200human GRCh37 chr7: 123,153,807-123,268,571 , GRCh38.p12 chr7: 123,513,753-123,628,517 IQUB, ASB15, 2 more genes
    nsv4820372copy number variation1nstd200human GRCh37 chr7: 123,123,907-123,126,167 , GRCh38.p12 chr7: 123,483,853-123,486,113 IQUB
    nsv4729428copy number variation1nstd102humanUncertain significance GRCh37 chr7: 122,963,176-123,347,717 , GRCh38.p12 chr7: 123,323,122-123,707,663 LMOD2, RNU6-296P, 5 more genes
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