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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979182inversion1nstd209human GRCh38 chr7: 99,981,419-101,289,122 , GRCh37.p13 chr7: 99,579,042-100,932,403 , ACHE, 92 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 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
    nsv4713287copy number variation1nstd195human GRCh37 chr7: 100,645,401-100,821,401 , GRCh38.p12 chr7: 101,002,120-101,178,120 MUC12, AP1S1, 8 more genes
    nsv4684274copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 99,593,346-102,470,275 , GRCh38.p12 chr7: 99,995,723-102,829,828 ACHE, AP1S1, 124 more genes
    nsv4601023copy number variation1nstd183human GRCh37 chr7: 100,715,874-101,148,415 , GRCh38.p12 chr7: 101,072,593-101,505,134 TRIM56, FIS1, 17 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
    nsv3922815copy number variation1nstd102humanPathogenic NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453 SEPTIN7P6, MIR93, 1175 more genes
    nsv3921918copy number variation1nstd102humanUncertain significance GRCh38 chr7: 99,932,610-102,473,188 , GRCh37 chr7: 99,530,233-102,113,635 , NCBI36 chr7: 99,368,169-101,900,640 MIR4285, SLC12A9-AS1, 114 more genes
    nsv3920604copy number variation1nstd102humanBenign GRCh38 chr7: 101,130,561-101,255,628 , NCBI36 chr7: 100,560,562-100,685,629 , GRCh37 chr7: 100,773,842-100,898,909 MOGAT3, FIS1, 10 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
    nsv3919108copy number variation1nstd102humanPathogenic GRCh38 chr7: 100,419,914-102,482,826 , NCBI36 chr7: 99,855,473-101,910,278 , GRCh37 chr7: 100,017,537-102,123,273 SPACDR, IRS3P, 80 more genes
    nsv3916333copy number variation1nstd102humanPathogenic GRCh37 chr7: 97,917,786-100,903,085 , GRCh38 chr7: 98,288,474-101,259,804 , NCBI36 chr7: 97,755,722-100,689,805 ZCWPW1, LOC101927610, 141 more genes
    nsv3915692copy number variation1nstd102humanPathogenic GRCh38 chr7: 99,195,836-102,258,175 , NCBI36 chr7: 98,631,395-101,688,175 , GRCh37 chr7: 98,793,459-101,718,950 MUC17, LOC107986829, 135 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
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