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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5579202copy number variation1nstd207human GRCh38 chr7: 95,312,720-95,312,784 , GRCh37.p13 chr7: 94,942,032-94,942,096 PON1
    nsv5561126sequence alteration1nstd206human GRCh38 chr7: 95,304,521-95,306,178 , GRCh37.p13 chr7: 94,933,833-94,935,490 PON1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 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
    nsv4957736copy number variation1nstd200human GRCh38 chr7: 95,310,424-95,338,769 , GRCh37.p13 chr7: 94,939,736-94,968,081 PON1
    nsv4957725copy number variation1nstd200human GRCh38 chr7: 94,948,777-95,365,497 , GRCh37.p13 chr7: 94,578,089-94,994,809 PON1, PON3, 5 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4819613copy number variation1nstd200human GRCh37 chr7: 94,578,089-94,994,809 , GRCh38.p12 chr7: 94,948,777-95,365,497 PON1, PON3, 5 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4685981copy number variation1nstd102humanPathogenic GRCh37 chr7: 93,516,132-95,668,733 , GRCh38.p12 chr7: 93,886,820-96,039,421 LOC105375404, BET1, 36 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
    nsv4383554copy number variation1nstd173human GRCh37 chr7: 94,814,740-95,060,242 , GRCh38.p12 chr7: 95,185,428-95,430,930 PON1, PON2, 5 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
    nsv4172074copy number variation1nstd166human GRCh37.p13 chr7: 94,943,440-94,943,877 , GRCh38.p12 chr7: 95,314,128-95,314,565 PON1
    nsv4164722copy number variation1nstd166human GRCh37.p13 chr7: 94,942,177-94,947,901 , GRCh38.p12 chr7: 95,312,865-95,318,589 PON1
    nsv4163756copy number variation1nstd166human GRCh37.p13 chr7: 94,933,570-94,934,072 , GRCh38.p12 chr7: 95,304,258-95,304,760 PON1
    nsv4162430copy number variation1nstd166human GRCh37.p13 chr7: 94,930,781-94,931,957 , GRCh38.p12 chr7: 95,301,469-95,302,645 PON1
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