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Items: 1 to 20 of 97

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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
    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
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 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
    nsv4675411copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,889,712-115,323,564 , GRCh38.p12 chr7: 114,249,657-115,683,510 SNORA25B, RNA5SP238, 9 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
    nsv4457161copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,898,185-115,322,759 , GRCh38.p12 chr7: 114,258,130-115,682,705 LINC01393, RNA5SP238, 9 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
    nsv4371191copy number variation1nstd173human GRCh37 chr7: 108,606,430-119,657,890 , GRCh38.p12 chr7: 108,966,373-120,017,836 , LOC100421901, 94 more genes
    nsv4166828copy number variation1nstd166human GRCh37.p13 chr7: 115,052,163-115,407,473 , GRCh38.p12 chr7: 115,412,109-115,767,419 LOC100506489, SNORA25B, 2 more genes
    nsv3924380copy number variation1nstd102humanPathogenic GRCh37 chr7: 101,912,320-120,918,695 , GRCh38 chr7: 102,196,924-121,278,641 , NCBI36 chr7: 101,626,924-120,705,931 LOC102724434, LRRN3, 222 more genes
    nsv3923570copy number variation1nstd102humanPathogenic NCBI36 chr7: 107,583,881-122,963,817 , GRCh37.p13 chr7: 107,796,645-123,176,581 , GRCh38.p12 chr7: 108,156,200-123,536,527 ANKRD7, NDUFA5, 142 more genes
    nsv3922815copy number variation1nstd102humanPathogenic NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453 SEPTIN7P6, MIR93, 1175 more genes
    nsv3922792copy number variation1nstd102humanPathogenic NCBI36 chr7: 113,227,126-124,326,508 , GRCh37 chr7: 113,439,890-124,539,272 , GRCh38 chr7: 113,799,835-124,899,218 MTND4P6, COMETT, 116 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
    nsv3918979copy number variation1nstd102humanPathogenic GRCh37 chr7: 115,099,069-159,118,507 , NCBI36 chr7: 114,886,305-158,811,268 , GRCh38 chr7: 115,459,015-159,325,817 ABCF2, LOC105375581, 844 more genes
    nsv3916529copy number variation1nstd102humanPathogenic GRCh37 chr7: 113,782,532-125,480,435 , NCBI36 chr7: 113,569,768-125,267,671 , GRCh38 chr7: 114,142,477-125,840,381 CAPZA2, LMOD2, 124 more genes
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