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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
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4968865copy number variation1nstd200human GRCh38 chr7: 140,900,967-141,043,981 , GRCh37.p13 chr7: 140,600,767-140,743,781 LOC107986720, MRPS33, 3 more genes
    nsv4966878copy number variation1nstd200human GRCh38 chr7: 141,005,282-141,005,921 , GRCh37.p13 chr7: 140,705,082-140,705,721 LOC105375536, MRPS33
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4869975inversion1nstd200human GRCh37 chr7: 140,214,312-141,993,227 , GRCh38.p12 chr7: 140,514,512-142,288,987 , TMEM178B, 44 more genes
    nsv4710490copy number variation1nstd195human GRCh37 chr7: 140,702,219-140,702,220 , GRCh38.p12 chr7: 141,002,419-141,002,420 MRPS33, LOC105375536
    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
    nsv4675615copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620 ATG9B, OR10AC1, 603 more genes
    nsv4599699copy number variation1nstd183human GRCh37 chr7: 140,601,875-140,742,109 , GRCh38.p12 chr7: 140,902,075-141,042,309 BRAF, MRPS33, 3 more genes
    nsv4570841mobile element insertion1nstd166human GRCh37.p13 chr7: 140,712,858-140,712,858 , GRCh38.p12 chr7: 141,013,058-141,013,058 MRPS33, LOC105375536
    nsv4455493copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,592,554-159,119,707 , GRCh38.p12 chr7: 130,907,795-159,327,017 OR2A1, LOC101027084, 614 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
    nsv4382751copy number variation1nstd173human GRCh37 chr7: 140,634,307-140,741,137 , GRCh38.p12 chr7: 140,934,507-141,041,337 LOC107986720, MRPS33, 2 more genes
    nsv4381639copy number variation1nstd173human GRCh37 chr7: 140,609,732-140,742,271 , GRCh38.p12 chr7: 140,909,932-141,042,471 MRPS33, LOC105375536, 3 more genes
    nsv4349183copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,312,450-159,119,220 , GRCh38.p12 chr7: 128,672,396-159,326,530 LOC105375582, TRBJ2-4, 686 more genes
    nsv3964459copy number variation1nstd168human GRCh38 chr7: 140,974,840-141,034,905 , GRCh37.p13 chr7: 140,674,640-140,734,705 CCT4P1, LOC107986720, 2 more genes
    nsv3924666copy number variation1nstd102humanUncertain significance GRCh38 chr7: 140,061,285-144,622,893 , NCBI36 chr7: 139,407,554-143,950,919 , GRCh37 chr7: 139,761,085-144,319,986 MKRN1, TRBV24-1, 234 more genes
    nsv3924585copy number variation1nstd102humanPathogenic NCBI36 chr7: 130,506,777-158,812,468 , GRCh38 chr7: 131,171,478-159,327,017 , GRCh37 chr7: 130,856,237-159,119,707 PAXBP1P1, RNY3, 611 more genes
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