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Items: 1 to 20 of 79

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924435copy number variation1nstd209human GRCh38 chr7: 99,610,771-99,611,705 , GRCh37.p13 chr7: 99,208,394-99,209,328 TMEM225B
    nsv5919008copy number variation1nstd209human GRCh38 chr7: 99,605,389-99,605,550 , GRCh37.p13 chr7: 99,203,012-99,203,173 TMEM225B
    nsv5909614copy number variation1nstd209human GRCh38 chr7: 99,586,538-99,586,913 , GRCh37.p13 chr7: 99,184,161-99,184,536 TMEM225B
    nsv5849606copy number variation1nstd209human GRCh38 chr7: 99,610,672-99,611,871 , GRCh37.p13 chr7: 99,208,295-99,209,494 TMEM225B
    nsv5575636copy number variation1nstd207human GRCh38 chr7: 99,605,389-99,605,550 , GRCh37.p13 chr7: 99,203,012-99,203,173 TMEM225B
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5480857copy number variation1nstd206human GRCh38 chr7: 99,610,775-99,611,706 , GRCh37.p13 chr7: 99,208,398-99,209,329 TMEM225B
    nsv5479159copy number variation1nstd206human GRCh38 chr7: 99,588,877-99,590,438 , GRCh37.p13 chr7: 99,186,500-99,188,061 TMEM225B
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5370853translocation1nstd200human GRCh38 chr7: 99,611,706-99,611,706 , GRCh38 chr7: 99,610,775-99,610,775 , GRCh37.p13 chr7: 99,208,398-99,208,398 , GRCh37.p13 chr7: 99,209,329-99,209,329 TMEM225B
    nsv5370852translocation1nstd200human GRCh38 chr7: 99,603,318-99,603,318 , GRCh38 chr7: 99,603,236-99,603,236 , GRCh37.p13 chr7: 99,200,859-99,200,859 , GRCh37.p13 chr7: 99,200,941-99,200,941 TMEM225B
    nsv5370851translocation1nstd200human GRCh38 chr7: 99,597,720-99,597,720 , GRCh38 chr7: 99,597,651-99,597,651 , GRCh37.p13 chr7: 99,195,274-99,195,274 , GRCh37.p13 chr7: 99,195,343-99,195,343 TMEM225B
    nsv5370850translocation1nstd200human GRCh38 chr7: 99,582,366-99,582,366 , GRCh38 chr7: 99,582,274-99,582,274 , GRCh37.p13 chr7: 99,179,989-99,179,989 , GRCh37.p13 chr7: 99,179,897-99,179,897 TMEM225B
    nsv5340314translocation1nstd200human GRCh37 chr7: 99,179,897-99,179,897 , GRCh37 chr7: 99,179,989-99,179,989 , GRCh38.p12 chr7: 99,582,274-99,582,274 , GRCh38.p12 chr7: 99,582,366-99,582,366 TMEM225B
    nsv5330127translocation1nstd200human GRCh37 chr7: 99,208,398-99,208,398 , GRCh37 chr7: 99,209,329-99,209,329 , GRCh38.p12 chr7: 99,611,706-99,611,706 , GRCh38.p12 chr7: 99,610,775-99,610,775 TMEM225B
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 more genes
    nsv5305896copy number variation1nstd204human GRCh37.p13 chr7: 99,166,505-99,279,863 , GRCh38.p13 chr7: 99,568,882-99,682,240 CYP3A5, ZNF655, 3 more genes
    nsv5259854copy number variation1nstd204human GRCh38.p13 chr7: 99,577,758-99,578,957 , GRCh37.p13 chr7: 99,175,381-99,176,580 TMEM225B
    nsv5258181copy number variation1nstd204human GRCh38.p13 chr7: 99,420,101-99,576,000 , GRCh37.p13 chr7: 99,017,724-99,173,623 TMEM225B, ZNF394, 13 more genes
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