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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5568765copy number variation1nstd207human GRCh38 chr7: 94,659,438-94,659,511 , GRCh37.p13 chr7: 94,288,750-94,288,823 PEG10
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 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
    nsv5381552copy number variation1nstd102humanUncertain significance GRCh37 chr7: 94,285,282-94,285,430 , GRCh38.p12 chr7: 94,655,970-94,656,118 SGCE, PEG10
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 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
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4748855copy number variation1nstd199human GRCh37 chr7: 94,288,744-94,288,817 , GRCh38.p12 chr7: 94,659,432-94,659,505 PEG10
    nsv4685981copy number variation1nstd102humanPathogenic GRCh37 chr7: 93,516,132-95,668,733 , GRCh38.p12 chr7: 93,886,820-96,039,421 LOC105375404, BET1, 36 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4155050copy number variation1nstd166human GRCh37.p13 chr7: 94,298,896-94,298,968 , GRCh38.p12 chr7: 94,669,584-94,669,656 PEG10
    nsv3949052copy number variation1nstd167human GRCh37 chr7: 94,288,750-94,288,824 , GRCh38.p12 chr7: 94,659,438-94,659,512 PEG10
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3916221copy number variation1nstd102humanPathogenic NCBI36 chr7: 92,754,488-94,797,369 , GRCh37.p13 chr7: 92,916,552-94,959,433 , GRCh38.p12 chr7: 93,287,240-95,330,121 BET1-AS1, RN7SKP129, 33 more genes
    nsv3914094copy number variation1nstd102humanPathogenic GRCh38 chr7: 84,002,634-95,228,883 , GRCh37 chr7: 83,631,950-94,858,195 , NCBI36 chr7: 83,469,886-94,696,131 LINC03017, MIR1285-1, 121 more genes
    nsv3911538copy number variation1nstd102humanPathogenic NCBI36 chr7: 92,226,394-97,035,894 , GRCh38 chr7: 92,759,144-97,568,646 , GRCh37 chr7: 92,388,458-97,197,958 LOC105375410, LOC107984034, 75 more genes
    nsv3909475copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 94,129,826-94,844,077 , GRCh38.p12 chr7: 94,500,514-95,214,765 SGCE, PEG10, 12 more genes
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