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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963567insertion1nstd209human GRCh38 chr7: 139,445,793-139,445,793 , GRCh37.p13 chr7: 139,130,539-139,130,539 KLRG2
    nsv5914832copy number variation1nstd209human GRCh38 chr7: 139,477,993-139,480,978 , GRCh37.p13 chr7: 139,162,739-139,165,724 KLRG2
    nsv5910049copy number variation1nstd209human GRCh38 chr7: 139,448,662-139,449,369 , GRCh37.p13 chr7: 139,133,408-139,134,115 KLRG2, RNU6-911P
    nsv5866889copy number variation1nstd209human GRCh38 chr7: 139,477,895-139,481,003 , GRCh37.p13 chr7: 139,162,641-139,165,749 KLRG2
    nsv5643665insertion1nstd207human GRCh38 chr7: 139,445,781-139,445,781 , GRCh37.p13 chr7: 139,130,527-139,130,527 KLRG2
    nsv5642559insertion1nstd207human GRCh38 chr7: 139,445,797-139,445,797 , GRCh37.p13 chr7: 139,130,543-139,130,543 KLRG2
    nsv5578863copy number variation1nstd207human GRCh38 chr7: 139,424,841-139,425,205 , GRCh37.p13 chr7: 139,109,587-139,109,951 LOC100129148, KLRG2
    nsv5566189copy number variation1nstd207human GRCh38 chr7: 139,448,558-139,449,129 , GRCh37.p13 chr7: 139,133,304-139,133,875 RNU6-911P, KLRG2
    nsv5558277sequence alteration1nstd206human GRCh38 chr7: 139,448,923-139,450,182 , GRCh37.p13 chr7: 139,133,669-139,134,928 KLRG2, RNU6-911P
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5486256copy number variation1nstd206human GRCh38 chr7: 139,448,558-139,449,150 , GRCh37.p13 chr7: 139,133,304-139,133,896 KLRG2, RNU6-911P
    nsv5482982copy number variation1nstd206human GRCh38 chr7: 139,424,856-139,425,206 , GRCh37.p13 chr7: 139,109,602-139,109,952 KLRG2, LOC100129148
    nsv5480261copy number variation1nstd206human GRCh38 chr7: 139,449,980-139,450,502 , GRCh37.p13 chr7: 139,134,726-139,135,248 KLRG2
    nsv5478348copy number variation1nstd206human GRCh38 chr7: 139,449,973-139,455,713 , GRCh37.p13 chr7: 139,134,719-139,140,459 KLRG2
    nsv5382472mobile element deletion1nstd186human GRCh37 chr7: 139,109,598-139,109,952 , GRCh38.p12 chr7: 139,424,852-139,425,206 KLRG2, LOC100129148
    nsv5371286translocation1nstd200human GRCh38 chr7: 139,448,582-139,448,582 , GRCh38 chr7: 139,449,130-139,449,130 , GRCh37.p13 chr7: 139,133,876-139,133,876 , GRCh37.p13 chr7: 139,133,328-139,133,328 RNU6-911P, KLRG2
    nsv5371285translocation1nstd200human GRCh38 chr7: 139,424,856-139,424,856 , GRCh38 chr7: 139,425,206-139,425,206 , GRCh37.p13 chr7: 139,109,602-139,109,602 , GRCh37.p13 chr7: 139,109,952-139,109,952 LOC100129148, KLRG2
    nsv5331470translocation1nstd200human GRCh37 chr7: 139,125,277-139,125,277 , GRCh37 chr7: 139,125,337-139,125,337 , GRCh38.p12 chr7: 139,440,591-139,440,591 , GRCh38.p12 chr7: 139,440,531-139,440,531 KLRG2
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5325114translocation1nstd204human GRCh37.p13 chr7: 139,109,602-139,109,602 , GRCh37.p13 chr7: 139,109,952-139,109,952 , GRCh38.p13 chr7: 139,424,856-139,424,856 , GRCh38.p13 chr7: 139,425,206-139,425,206 KLRG2, LOC100129148
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