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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914456copy number variation1nstd209human GRCh38 chr7: 128,499,704-128,999,795 , GRCh37.p13 chr7: 128,139,758-128,639,849 , KCP, 25 more genes
    nsv5911338copy number variation1nstd209human GRCh38 chr7: 128,499,612-128,999,703 , GRCh37.p13 chr7: 128,139,666-128,639,757 , CICP14, 25 more genes
    nsv5847938copy number variation1nstd209human GRCh38 chr7: 128,852,683-128,853,782 , GRCh37.p13 chr7: 128,492,737-128,493,836 FLNC-AS1, FLNC
    nsv5674026copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,469,483-128,500,328 , GRCh38.p12 chr7: 128,829,429-128,860,274 FLNC, FLNC-AS1
    nsv5673787copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 128,475,370-128,478,867 , GRCh38.p12 chr7: 128,835,316-128,838,813 FLNC
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5381397copy number variation1nstd102humanUncertain significance GRCh37 chr7: 128,470,672-128,498,597 , GRCh38.p12 chr7: 128,830,618-128,858,543 FLNC-AS1, FLNC
    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
    nsv4682955copy number variation1nstd102humanUncertain significance GRCh37 chr7: 128,475,370-128,498,587 , GRCh38.p12 chr7: 128,835,316-128,858,533 FLNC-AS1, FLNC
    nsv4682891copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,488,605-128,489,046 , GRCh38.p12 chr7: 128,848,551-128,848,992 FLNC-AS1, FLNC
    nsv4681823copy number variation1nstd102humanUncertain significance GRCh37 chr7: 128,482,275-128,490,138 , GRCh38.p12 chr7: 128,842,221-128,850,084 FLNC, FLNC-AS1
    nsv4681161copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr7: 128,470,682-128,498,587 , GRCh38.p12 chr7: 128,830,628-128,858,533 FLNC, FLNC-AS1
    nsv4681077copy number variation1nstd102humanUncertain significance GRCh37 chr7: 128,498,380-128,498,587 , GRCh38.p12 chr7: 128,858,326-128,858,533 FLNC-AS1, FLNC
    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
    nsv4658851copy number variation1nstd186human GRCh37 chr7: 128,469,851-128,474,907 , GRCh38.p12 chr7: 128,829,797-128,834,853 FLNC
    nsv4602823copy number variation1nstd183human GRCh37 chr7: 128,418,055-128,592,817 , GRCh38.p12 chr7: 128,778,001-128,952,763 , LOC105375497, 10 more genes
    nsv4599648copy number variation1nstd183human GRCh37 chr7: 128,469,851-128,474,907 , GRCh38.p12 chr7: 128,829,797-128,834,853 FLNC
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