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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5679876mobile element insertion1nstd211human GRCh38 chr7: 118,235,923-118,235,923 , GRCh37.p13 chr7: 117,875,977-117,875,977 ANKRD7
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5481423copy number variation1nstd206human GRCh38 chr7: 118,239,431-118,268,250 , GRCh37.p13 chr7: 117,879,485-117,908,304 LOC102724495, ANKRD7
    nsv5412627mobile element insertion1nstd206human GRCh38 chr7: 118,235,923-118,235,974 , GRCh37.p13 chr7: 117,875,977-117,876,028 ANKRD7
    nsv5381759copy number variation1nstd102humanPathogenic GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640 TMEM229A, ST7-OT3, 110 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5108704mobile element insertion1nstd203human GRCh38 chr7: 118,241,536-118,241,549 , GRCh37.p13 chr7: 117,881,590-117,881,603 ANKRD7
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5037184inversion1nstd200human GRCh37.p13 chr7: 117,848,998-118,342,777 , GRCh38 chr7: 118,208,944-118,702,723 ANKRD7, LOC102724495, 4 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4965194copy number variation1nstd200human GRCh38 chr7: 117,743,324-119,522,445 , GRCh37.p13 chr7: 117,383,378-119,162,499 LSM8, ANKRD7, 9 more genes
    nsv4957849copy number variation1nstd200human GRCh38 chr7: 118,217,614-118,253,115 , GRCh37.p13 chr7: 117,857,668-117,893,169 ANKRD7
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4820245copy number variation1nstd200human GRCh37 chr7: 117,871,502-117,884,036 , GRCh38.p12 chr7: 118,231,448-118,243,982 ANKRD7
    nsv4820244copy number variation1nstd200human GRCh37 chr7: 117,857,668-117,893,169 , GRCh38.p12 chr7: 118,217,614-118,253,115 ANKRD7
    nsv4761009insertion1nstd199human GRCh37 chr7: 117,875,976-117,875,976 , GRCh38.p12 chr7: 118,235,922-118,235,922 ANKRD7
    nsv4679903copy number variation1nstd189human GRCh37.p13 chr7: 117,637,563-118,059,838 , GRCh38.p12 chr7: 117,997,509-118,419,784 LSM8, ANKRD7, 2 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4675322copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,617,406-123,217,914 , GRCh38.p12 chr7: 106,976,961-123,577,860 CBLL1-AS1, COMETT, 168 more genes
    nsv4603859copy number variation1nstd183human GRCh37 chr7: 117,874,917-117,875,991 , GRCh38.p12 chr7: 118,234,863-118,235,937 ANKRD7
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