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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975022inversion1nstd209human GRCh38 chr7: 34,818,028-37,653,165 , GRCh37.p13 chr7: 34,857,640-37,692,768 , AOAH, 41 more genes
    nsv5914132copy number variation1nstd209human GRCh38 chr7: 26,936,027-36,716,695 , GRCh37.p13 chr7: 26,975,646-36,756,300 , HOXA7, 162 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5486618copy number variation1nstd206human GRCh38 chr7: 35,784,000-35,790,242 , GRCh37.p13 chr7: 35,823,610-35,829,852 SEPTIN7-DT
    nsv5113626mobile element insertion1nstd203human GRCh38 chr7: 35,789,912-35,789,923 , GRCh37.p13 chr7: 35,829,522-35,829,533 SEPTIN7-DT
    nsv5101286mobile element insertion1nstd203human GRCh38 chr7: 35,759,141-35,759,154 , GRCh37.p13 chr7: 35,798,751-35,798,764 SEPTIN7-DT
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5034601inversion1nstd200human GRCh38 chr7: 35,767,212-35,767,537 , GRCh37.p13 chr7: 35,806,822-35,807,147 SEPTIN7-DT, LOC442293
    nsv5031433inversion1nstd200human GRCh38 chr7: 35,767,228-35,767,852 , GRCh37.p13 chr7: 35,806,838-35,807,462 SEPTIN7-DT, LOC442293
    nsv4966176copy number variation1nstd200human GRCh38 chr7: 35,769,480-35,774,621 , GRCh37.p13 chr7: 35,809,090-35,814,231 SEPTIN7-DT
    nsv4966175copy number variation1nstd200human GRCh38 chr7: 35,768,428-35,770,147 , GRCh37.p13 chr7: 35,808,038-35,809,757 LOC442293, SEPTIN7-DT
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4811318copy number variation1nstd200human GRCh37 chr7: 35,808,038-35,809,757 , GRCh38.p12 chr7: 35,768,428-35,770,147 SEPTIN7-DT, LOC442293
    nsv4811317copy number variation1nstd200human GRCh37 chr7: 35,794,775-35,795,200 , GRCh38.p12 chr7: 35,755,165-35,755,590 SEPTIN7-DT
    nsv4787204mobile element deletion1nstd200human GRCh37 chr7: 35,818,224-35,818,520 , GRCh38.p12 chr7: 35,778,614-35,778,910 SEPTIN7-DT
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4337262sequence alteration1nstd166human GRCh37.p13 chr7: 35,806,821-35,807,462 , GRCh38.p12 chr7: 35,767,211-35,767,852 LOC442293, SEPTIN7-DT
    nsv4148199copy number variation1nstd166human GRCh37.p13 chr7: 35,794,775-35,795,228 , GRCh38.p12 chr7: 35,755,165-35,755,618 SEPTIN7-DT
    nsv4139896copy number variation1nstd166human GRCh37.p13 chr7: 35,808,038-35,809,809 , GRCh38.p12 chr7: 35,768,428-35,770,199 LOC442293, SEPTIN7-DT
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