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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv4685991copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 95,911,538-97,301,820 , GRCh38.p12 chr7: 96,282,226-97,672,508 DLX5, DLX6, 22 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
    nsv3922980copy number variation1nstd102humanPathogenic GRCh37 chr7: 94,756,382-97,502,799 , GRCh38 chr7: 95,127,070-97,873,487 , NCBI36 chr7: 94,594,318-97,340,735 RNU6-532P, DLX6-AS1, 41 more genes
    nsv3919858copy number variation1nstd102humanPathogenic NCBI36 chr7: 96,391,401-96,624,516 , GRCh37 chr7: 96,553,465-96,786,580 , GRCh38 chr7: 96,924,153-97,157,268 DLX5, DLX6, 5 more genes
    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
    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
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 MNX1-AS2, VN1R31P, 2682 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 TRGV3, SNX10-AS1, 2682 more genes
    nsv3901032copy number variation1nstd102humanPathogenic GRCh37 chr7: 93,700,162-96,950,914 , GRCh38.p12 chr7: 94,070,850-97,321,602 LOC105375404, LOC107984034, 52 more genes
    nsv3899656copy number variation1nstd102humanUncertain significance GRCh37 chr7: 96,066,104-97,428,089 , GRCh38.p12 chr7: 96,436,792-97,798,777 LOC107984034, LOC107986825, 18 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 RNU6-565P, LAMB1, 2684 more genes
    nsv3892887copy number variation1nstd102humanPathogenic GRCh37 chr7: 92,445,452-99,686,985 , GRCh38.p12 chr7: 92,816,138-100,089,362 LOC105375402, LOC112267858, 153 more genes
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