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Items: 1 to 20 of 774

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7148154copy number variation1nstd102humanPathogenic GRCh38 chr7: 154,446,117-159,206,757 , GRCh37.p13 chr7: 154,143,202-158,999,446 LOC105375602, LOC105375599, 70 more genes
    nsv7143975insertion1nstd232human GRCh37.p13 chr7: 158,424,411-158,424,411 , GRCh38.p12 chr7: 158,631,719-158,631,719 NCAPG2
    nsv7141168insertion1nstd232human GRCh37.p13 chr7: 158,448,369-158,448,369 , GRCh38.p12 chr7: 158,655,677-158,655,677 NCAPG2
    nsv7140321insertion1nstd232human GRCh37.p13 chr7: 158,430,202-158,430,202 , GRCh38.p12 chr7: 158,637,510-158,637,510 NCAPG2
    nsv7137486insertion1nstd232human GRCh37.p13 chr7: 158,448,149-158,448,149 , GRCh38.p12 chr7: 158,655,457-158,655,457 NCAPG2
    nsv7097356copy number variation2nstd102humanPathogenic GRCh37 chr7: 152,617,597-158,500,659 , GRCh38.p12 chr7: 152,920,512-158,707,968 LOC107986722, LOC105375593, 76 more genes
    nsv7077957inversion1nstd229human GRCh38 chr7: 158,614,485-158,932,635 , GRCh37.p13 chr7: 158,407,177-158,725,326 NCAPG2, ESYT2, 3 more genes
    nsv7074785inversion1nstd229human GRCh38 chr7: 157,888,655-159,201,386 , GRCh37.p13 chr7: 157,681,347-158,994,075 PTPRN2, LINC01022, 10 more genes
    nsv7072410inversion1nstd229human GRCh38 chr7: 158,587,702-158,721,193 , GRCh37.p13 chr7: 158,380,394-158,513,884 LINC01022, NCAPG2, 4 more genes
    nsv7064300inversion1nstd229human GRCh38 chr7: 158,614,484-158,938,027 , GRCh37.p13 chr7: 158,407,176-158,730,718 NCAPG2, ESYT2, 3 more genes
    nsv7063608inversion1nstd229human GRCh38 chr7: 158,631,512-158,999,431 , GRCh37.p13 chr7: 158,424,204-158,792,122 DYNC2I1, RPL21P76, 2 more genes
    nsv7061552inversion1nstd229human GRCh38 chr7: 158,636,871-158,660,752 , GRCh37.p13 chr7: 158,429,563-158,453,444 NCAPG2
    nsv6838040copy number variation1nstd229human GRCh38 chr7: 158,676,377-158,794,601 , GRCh37.p13 chr7: 158,469,069-158,587,292 NCAPG2, RPL21P76, 1 more genes
    nsv6837988copy number variation1nstd229human GRCh38 chr7: 158,635,186-158,638,628 , GRCh37.p13 chr7: 158,427,878-158,431,320 NCAPG2
    nsv6831809copy number variation1nstd229human GRCh38 chr7: 158,408,734-158,834,438 , GRCh37.p13 chr7: 158,201,426-158,627,129 NCAPG2, RPL21P76, 6 more genes
    nsv6831469copy number variation1nstd229human GRCh38 chr7: 158,660,414-158,679,442 , GRCh37.p13 chr7: 158,453,106-158,472,134 NCAPG2
    nsv6831365copy number variation1nstd229human GRCh38 chr7: 158,645,677-158,941,685 , GRCh37.p13 chr7: 158,438,369-158,734,376 DYNC2I1, ESYT2, 2 more genes
    nsv6829656copy number variation1nstd229human GRCh38 chr7: 158,634,705-158,642,364 , GRCh37.p13 chr7: 158,427,397-158,435,056 NCAPG2
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