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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5847341copy number variation2nstd209human GRCh38 chr7: 57,170,918-57,172,017 , GRCh37.p13 chr7: 57,238,625-57,239,724 MTND4P4, MTND5P6, 3 more genes
    nsv5846759copy number variation2nstd209human GRCh38 chr7: 57,174,427-57,182,421 , GRCh37.p13 chr7: 57,242,134-57,250,128 GUSBP10, MTCYBP29
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5490569copy number variation1nstd206human GRCh38 chr7: 57,174,836-57,198,229 , GRCh37.p13 chr7: 57,242,543-57,265,936 MTND4LP4, MTCO3P4, 11 more genes
    nsv5482153copy number variation1nstd206human GRCh38 chr7: 56,993,800-57,540,242 , GRCh37.p13 chr7: 57,190,580-57,599,948 , MTCYBP29, 39 more genes
    nsv5237787copy number variation1nstd204human GRCh37.p13 chr7: 57,234,208-57,242,007 , GRCh38.p13 chr7: 57,166,501-57,174,300 GUSBP10, MTND4P4, 5 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4964674copy number variation1nstd200human GRCh38 chr7: 57,167,958-57,191,370 , GRCh37.p13 chr7: 57,235,665-57,259,077 MTND4P5, MTCO3P10, 14 more genes
    nsv4956893copy number variation1nstd200human GRCh38 chr7: 57,144,009-57,418,681 , GRCh37.p13 chr7|NW_003571038.1: 1-144,162 , MTND4P5, 27 more genes
    nsv4956891copy number variation1nstd200human GRCh38 chr7: 57,056,195-63,228,539 , GRCh37.p13 chr7: 57,190,578-62,688,917 , SEPTIN7P15, 50 more genes
    nsv4828959copy number variation1nstd200human GRCh37 chr7: 57,235,608-57,259,030 , GRCh38.p12 chr7: 57,167,901-57,191,323 MTND4P5, MTND1P4, 14 more genes
    nsv4819075copy number variation1nstd200human GRCh37 chr7: 57,211,716-57,478,393 , GRCh38.p12 chr7: 57,144,009-57,418,681 , MTATP6P8, 27 more genes
    nsv4765725inversion1nstd199human GRCh37 chr7: 57,119,077-62,979,736 , GRCh38.p12 chr7: 57,051,370-63,519,358 , ZNF479, 70 more genes
    nsv4761040inversion1nstd199human GRCh37 chr7: 55,830,732-65,288,125 , GRCh38.p12 chr7: 55,763,039-65,823,138 , CCT6A, 247 more genes
    nsv4684255copy number variation1nstd102humanUncertain significance GRCh37 chr7: 57,127,051-57,528,311 , GRCh38.p12 chr7: 57,059,344-57,468,605 MTATP6P8, NMTRQ-TTG13-1, 33 more genes
    nsv4679115copy number variation1nstd189human GRCh37.p13 chr7: 56,818,765-57,582,095 , GRCh38.p12 chr7: 56,751,072-57,522,389 , ZNF479, 53 more genes
    nsv4616458copy number variation1nstd183human GRCh37 chr7: 57,239,203-57,262,571 , GRCh38.p12 chr7: 57,171,496-57,194,864 MTCYBP29, MTND4P5, 13 more genes
    nsv4612767copy number variation1nstd183human GRCh37 chr7: 56,701,214-58,007,147 , GRCh38.p12 chr7: 56,633,521-57,947,441 , LOC105375289, 66 more genes
    nsv4608784copy number variation1nstd183human GRCh37 chr7: 56,697,186-58,019,983 , GRCh38.p12 chr7: 56,629,493-57,960,277 , VN1R26P, 67 more genes
    nsv4604087copy number variation1nstd183human GRCh37 chr7: 57,130,914-57,863,811 , GRCh38.p12 chr7: 57,063,207-57,804,105 , SAPCD2P2, 40 more genes
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