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Items: 1 to 20 of 143

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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
    nsv5476135copy number variation1nstd206human GRCh38 chr7: 101,622,503-101,622,576 , GRCh37.p13 chr7: 101,265,783-101,265,856 MYL10
    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
    nsv4965064copy number variation1nstd200human GRCh38 chr7: 101,526,138-101,698,762 , GRCh37.p13 chr7: 101,169,419-101,342,042 , LOC107986832, 3 more genes
    nsv4965057copy number variation1nstd200human GRCh38 chr7: 101,291,401-102,143,126 , GRCh37.p13 chr7: 100,934,682-101,718,950 , CUX1, 7 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
    nsv4712656copy number variation1nstd195human GRCh37 chr7: 101,156,851-101,288,901 , GRCh38.p12 chr7: 101,513,570-101,645,621 , MYL10, 3 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
    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
    nsv4323299inversion1nstd166human GRCh37.p13 chr7: 100,902,917-101,342,141 , GRCh38.p12 chr7: 101,259,636-101,698,861 , EMSLR, 8 more genes
    nsv4169843copy number variation1nstd166human GRCh37.p13 chr7: 101,263,712-101,264,614 , GRCh38.p12 chr7: 101,620,432-101,621,334 MYL10
    nsv4169286copy number variation1nstd166human GRCh37.p13 chr7: 101,237,000-101,293,000 , GRCh38.p12 chr7: 101,593,720-101,649,720 MYL10
    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
    nsv3920103copy number variation1nstd102humanPathogenic NCBI36 chr7: 100,955,796-104,860,145 , GRCh38 chr7: 101,525,795-105,432,462 , GRCh37 chr7: 101,169,076-105,072,909 RNU6-1322P, PRKRIP1, 66 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
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