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Items: 1 to 20 of 96

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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
    nsv5482290copy number variation1nstd206human GRCh38 chr7: 50,485,836-50,575,163 , GRCh37.p13 chr7: 50,553,534-50,642,860 DDC, DDC-AS1
    nsv5480009copy number variation1nstd206human GRCh38 chr7: 50,532,891-50,533,319 , GRCh37.p13 chr7: 50,600,589-50,601,017 DDC, DDC-AS1
    nsv5309039copy number variation1nstd204human GRCh37.p13 chr7: 50,600,656-50,600,812 , GRCh38.p13 chr7: 50,532,958-50,533,114 DDC-AS1, DDC
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4964643copy number variation1nstd200human GRCh38 chr7: 50,496,899-50,713,944 , GRCh37.p13 chr7: 50,564,597-50,781,641 DDC, DDC-AS1, 1 more genes
    nsv4811643copy number variation1nstd200human GRCh37 chr7: 50,600,589-50,601,017 , GRCh38.p12 chr7: 50,532,891-50,533,319 DDC, DDC-AS1
    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
    nsv4147460copy number variation1nstd166human GRCh37.p13 chr7: 50,602,714-50,602,785 , GRCh38.p12 chr7: 50,535,016-50,535,087 DDC, DDC-AS1
    nsv3955819copy number variation1nstd168human GRCh38 chr7: 50,517,763-50,540,577 , GRCh37.p13 chr7: 50,585,461-50,608,275 DDC-AS1, DDC
    nsv3924054copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,573,756-56,174,815 , NCBI36 chr7: 40,540,281-56,142,309 , GRCh38 chr7: 40,534,157-56,107,122 VOPP1-DT, SGO1P2, 229 more genes
    nsv3919937copy number variation1nstd102humanPathogenic GRCh38 chr7: 44,571,949-53,699,760 , GRCh37 chr7: 44,611,548-53,767,453 , NCBI36 chr7: 44,578,073-53,734,947 LOC105375262, LOC105375259, 106 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
    nsv3917263copy number variation1nstd102humanPathogenic GRCh38 chr7: 33,328,312-62,377,476 , GRCh37 chr7: 33,367,924-61,831,899 , NCBI36 chr7: 33,334,449-61,469,334 MIR4649, LOC107986794, 444 more genes
    nsv3911166copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,060,197-50,611,198 , NCBI36 chr7: 40,026,722-50,578,692 , GRCh38 chr7: 40,020,598-50,543,500 SUGCT, C7orf57, 155 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
    nsv3899194copy number variation1nstd102humanPathogenic GRCh37 chr7: 11,048,840-52,863,626 , GRCh38.p12 chr7: 11,009,213-52,795,933 BRWD1P3, TRGV10, 590 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
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