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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960439insertion1nstd209human GRCh38 chr7: 116,498,945-116,498,945 , GRCh37.p13 chr7: 116,138,999-116,138,999 CAV2, LOC107986838
    nsv5686019mobile element insertion1nstd211human GRCh38 chr7: 116,503,950-116,503,950 , GRCh37.p13 chr7: 116,144,004-116,144,004 CAV2
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5371056translocation1nstd200human GRCh38 chr7: 116,505,005-116,505,005 , GRCh38 chr7: 116,503,478-116,503,478 , GRCh37.p13 chr7: 116,143,532-116,143,532 , GRCh37.p13 chr7: 116,145,059-116,145,059 CAV2
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5319533copy number variation1nstd204human GRCh38.p13 chr7: 116,508,615-116,516,555 , GRCh37.p13 chr7: 116,148,669-116,156,609 CAV2
    nsv5253469copy number variation1nstd204human GRCh38.p13 chr7: 116,508,814-116,516,709 , GRCh37.p13 chr7: 116,148,868-116,156,763 CAV2
    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
    nsv4965189copy number variation1nstd200human GRCh38 chr7: 116,498,734-116,507,671 , GRCh37.p13 chr7: 116,138,788-116,147,725 LOC107986838, CAV2
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4820213copy number variation1nstd200human GRCh37 chr7: 116,148,678-116,156,600 , GRCh38.p12 chr7: 116,508,624-116,516,546 CAV2
    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
    nsv4675193copy number variation1nstd102humanUncertain significance GRCh37 chr7: 116,084,558-116,289,829 , GRCh38.p12 chr7: 116,444,504-116,649,775 CAV1, CAV2, 2 more genes
    nsv4614367copy number variation1nstd183human GRCh37 chr7: 116,146,669-116,148,688 , GRCh38.p12 chr7: 116,506,615-116,508,634 CAV2
    nsv4600039copy number variation1nstd183human GRCh37 chr7: 116,146,669-116,153,362 , GRCh38.p12 chr7: 116,506,615-116,513,308 CAV2
    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
    nsv4455068copy number variation1nstd102humanUncertain significance GRCh37 chr7: 115,892,116-116,371,242 , GRCh38.p12 chr7: 116,252,062-116,731,188 TES, CAV1, 6 more genes
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