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Items: 1 to 20 of 87

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673851copy number variation1nstd102humanPathogenic GRCh37 chr7: 91,829,918-91,851,387 , GRCh38.p12 chr7: 92,200,604-92,222,073 MIR1285-1, KRIT1
    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
    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
    nsv4964960copy number variation1nstd200human GRCh38 chr7: 92,148,896-92,215,642 , GRCh37.p13 chr7: 91,778,210-91,844,956 KRIT1, LRRD1, 2 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4825162copy number variation1nstd200human GRCh37 chr7: 91,778,210-91,844,956 , GRCh38.p12 chr7: 92,148,896-92,215,642 CYP51A1-AS1, MIR1285-1, 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
    nsv4675410copy number variation1nstd102humanPathogenic GRCh37 chr7: 91,809,746-91,836,087 , GRCh38.p12 chr7: 92,180,432-92,206,773 MIR1285-1, KRIT1, 1 more genes
    nsv4457252copy number variation1nstd102humanUncertain significance GRCh37 chr7: 91,779,899-91,856,816 , GRCh38.p12 chr7: 92,150,585-92,227,502 KRIT1, LRRD1, 2 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
    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
    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
    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
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 RNU6-565P, LAMB1, 2684 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 LOC107986817, DNAJB9, 2014 more genes
    nsv3881028copy number variation1nstd102humanUncertain significance GRCh37 chr7: 91,570,394-92,085,896 , GRCh38 chr7: 91,941,080-92,456,582 CYP51A1, LRRD1, 8 more genes
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