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Items: 1 to 20 of 137

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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
    nsv5487127copy number variation1nstd206human GRCh38 chr7: 116,953,912-116,958,062 , GRCh37.p13 chr7: 116,593,966-116,598,116 ST7, ST7-AS1, 1 more genes
    nsv5485753copy number variation1nstd206human GRCh38 chr7: 116,915,590-116,967,007 , GRCh37.p13 chr7: 116,555,644-116,607,061 CAPZA2, ST7, 4 more genes
    nsv5483992copy number variation1nstd206human GRCh38 chr7: 116,905,386-117,056,371 , GRCh37.p13 chr7: 116,545,440-116,696,425 CAPZA2, ST7, 6 more genes
    nsv5483568copy number variation1nstd206human GRCh38 chr7: 116,953,760-116,953,826 , GRCh37.p13 chr7: 116,593,814-116,593,880 ST7, ST7-AS1, 1 more genes
    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
    nsv5381393copy number variation1nstd102humanUncertain significance GRCh37 chr7: 116,339,139-117,307,162 , GRCh38.p12 chr7: 116,699,085-117,667,108 LOC105375466, MIR6132, 21 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
    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
    nsv4968658copy number variation1nstd200human GRCh38 chr7: 116,953,060-117,011,521 , GRCh37.p13 chr7: 116,593,114-116,651,575 ST7, TPM3P1, 2 more genes
    nsv4965193copy number variation1nstd200human GRCh38 chr7: 116,905,386-117,056,371 , GRCh37.p13 chr7: 116,545,440-116,696,425 TPM3P1, ST7-OT4, 6 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4682036copy number variation1nstd102humanUncertain significance GRCh37 chr7: 116,339,129-117,307,172 , GRCh38.p12 chr7: 116,699,075-117,667,118 MTND4P6, CFTR-AS1, 21 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
    nsv4661033copy number variation1nstd186human GRCh37 chr7: 116,594,099-116,598,083 , GRCh38.p12 chr7: 116,954,045-116,958,029 ST7, ST7-AS1, 1 more genes
    nsv4618260copy number variation1nstd183human GRCh37 chr7: 116,594,099-116,598,083 , GRCh38.p12 chr7: 116,954,045-116,958,029 ST7, ST7-AS1, 1 more genes
    nsv4455557copy number variation1nstd102humanPathogenic GRCh37 chr7: 107,410,314-117,825,549 , GRCh38.p12 chr7: 107,769,869-118,185,495 RAC1P6, LOC101928012, 103 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
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