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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977915inversion1nstd209human GRCh38 chr7: 86,525,777-88,855,329 , GRCh37.p13 chr7: 86,155,093-88,484,643 , GRM3, 31 more genes
    nsv5973961inversion1nstd209human GRCh37.p13 chr7: 87,707,926-88,185,252 , GRCh38 chr7: 88,078,611-88,555,937 SRI, ADAM22, 7 more genes
    nsv5923093copy number variation1nstd209human GRCh38 chr7: 88,506,706-88,626,926 , GRCh37.p13 chr7: 88,136,021-88,256,240 KPNA2P2, PET117P1, 2 more genes
    nsv5863048copy number variation1nstd209human GRCh38 chr7: 88,506,678-88,538,095 , GRCh37.p13 chr7: 88,135,993-88,167,410 PET117P1, LOC100419447
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5478646copy number variation1nstd206human GRCh38 chr7: 88,512,869-88,525,145 , GRCh37.p13 chr7: 88,142,184-88,154,460 PET117P1, LOC100419447
    nsv5477046copy number variation1nstd206human GRCh38 chr7: 88,506,708-88,626,927 , GRCh37.p13 chr7: 88,136,023-88,256,241 PET117P1, LOC100419447, 2 more genes
    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
    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
    nsv4950528copy number variation1nstd200human GRCh38 chr7: 88,494,048-90,880,305 , GRCh37.p13 chr7: 88,123,363-90,509,620 , LOC100419447, 25 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4819475copy number variation1nstd200human GRCh37 chr7: 88,136,023-88,256,241 , GRCh38.p12 chr7: 88,506,708-88,626,927 KPNA2P2, LOC100419447, 2 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4680837copy number variation1nstd189human GRCh37.p13 chr7: 88,113,722-89,885,076 , GRCh38.p12 chr7: 88,484,407-90,255,762 STEAP1, CFAP69, 15 more genes
    nsv4680423copy number variation1nstd189human GRCh37.p13 chr7: 88,121,267-89,894,589 , GRCh38.p12 chr7: 88,491,952-90,265,275 STEAP1, CFAP69, 15 more genes
    nsv4680245copy number variation1nstd189human GRCh37.p13 chr7: 88,109,532-89,826,168 , GRCh38.p12 chr7: 88,480,217-90,196,854 STEAP1, TEX47, 12 more genes
    nsv4679365copy number variation1nstd189human GRCh37.p13 chr7: 88,109,747-89,942,974 , GRCh38.p12 chr7: 88,480,432-90,313,660 STEAP1, CFAP69, 15 more genes
    nsv4616648copy number variation1nstd183human GRCh37 chr7: 88,142,185-88,154,461 , GRCh38.p12 chr7: 88,512,870-88,525,146 PET117P1, LOC100419447
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
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