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Items: 1 to 20 of 173

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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
    nsv5482153copy number variation1nstd206human GRCh38 chr7: 56,993,800-57,540,242 , GRCh37.p13 chr7: 57,190,580-57,599,948 , MTCYBP29, 39 more genes
    nsv5370590translocation1nstd200human GRCh38 chr7: 57,406,014-57,406,014 , GRCh38 chr7: 57,404,885-57,404,885 , GRCh37.p13 chr7|NW_003571038.1: 130,366-130,366 , GRCh37.p13 chr7|NW_003571038.1: 131,495-131,495 , GRCh37.p13 chr7: 57,472,591-57,472,591 , GRCh37.p13 chr7: 57,473,720-57,473,720 MIR3147, MIR3147HG
    nsv5370589translocation1nstd200human GRCh38 chr7: 57,406,024-57,406,024 , GRCh38 chr7: 57,404,677-57,404,677 , GRCh37.p13 chr7: 57,472,383-57,472,383 , GRCh37.p13 chr7: 57,473,730-57,473,730 , GRCh37.p13 chr7|NW_003571038.1: 130,158-130,158 , GRCh37.p13 chr7|NW_003571038.1: 131,505-131,505 MIR3147HG, MIR3147
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4964677copy number variation1nstd200human GRCh38 chr7: 57,405,339-57,409,212 , GRCh37.p13 chr7: 57,473,045-57,476,928 , GRCh37.p13 chr7|NW_003571038.1: 130,820-134,693 MIR3147, MIR3147HG
    nsv4964675copy number variation1nstd200human GRCh38 chr7: 57,185,639-57,823,153 , GRCh37.p13 chr7: 57,253,346-57,882,859 LOC105375297, GUSBP12, 27 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
    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
    nsv4679320copy number variation1nstd189human GRCh37.p13 chr7: 57,247,382-57,878,326 , GRCh38.p12 chr7: 57,179,675-57,818,620 ZNF716, SAPCD2P2, 28 more genes
    nsv4679259copy number variation1nstd189human GRCh37.p13 chr7: 57,247,056-58,022,431 , GRCh38.p12 chr7: 57,179,349-57,962,725 ZNF716, SAPCD2P2, 30 more genes
    nsv4679234copy number variation1nstd189human GRCh37.p13 chr7: 57,260,933-57,906,717 , GRCh38.p12 chr7: 57,193,226-57,847,011 ZNF716, SAPCD2P2, 20 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
    nsv4675898copy number variation1nstd102humanLikely benign GRCh37 chr7: 57,252,805-57,923,840 , GRCh38.p12 chr7: 57,185,098-57,864,134 MTND5P7, MIR3147, 29 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
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