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Items: 1 to 20 of 149

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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
    nsv5676906mobile element insertion1nstd211human GRCh38 chr7: 101,233,794-101,233,794 , GRCh37.p13 chr7: 100,877,075-100,877,075 CLDN15
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5493043copy number variation1nstd206human GRCh38 chr7: 101,237,223-101,237,321 , GRCh37.p13 chr7: 100,880,504-100,880,602 CLDN15
    nsv5489268copy number variation1nstd206human GRCh38 chr7: 101,208,460-101,267,760 , GRCh37.p13 chr7: 100,851,741-100,911,041 ZNHIT1, FIS1, 2 more genes
    nsv5489211copy number variation1nstd206human GRCh38 chr7: 101,227,197-101,230,157 , GRCh37.p13 chr7: 100,870,478-100,873,438 CLDN15
    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
    nsv4715293copy number variation1nstd195human GRCh37 chr7: 100,821,451-101,001,201 , GRCh38.p12 chr7: 101,178,170-101,357,920 PLOD3, NAT16, 11 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
    nsv4332494sequence alteration1nstd166human GRCh37.p13 chr7: 100,873,500-100,918,711 , GRCh38.p12 chr7: 101,230,219-101,275,430 CLDN15, FIS1, 1 more genes
    nsv4153128copy number variation1nstd166human GRCh37.p13 chr7: 100,880,504-100,880,602 , GRCh38.p12 chr7: 101,237,223-101,237,321 CLDN15
    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
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