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Items: 1 to 20 of 336

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047334inversion1nstd229human GRCh38 chr5: 119,494,072-128,765,801 , GRCh37.p13 chr5: 118,829,767-128,101,494 RPL18P3, KRT18P16, 98 more genes
    nsv7039392inversion1nstd229human GRCh38 chr5: 120,520,478-123,368,624 , GRCh37.p13 chr5: 119,856,173-122,704,318 PPIC-AS1, LOC101927357, 34 more genes
    nsv7039193inversion1nstd229human GRCh38 chr5: 122,429,373-122,429,459 , GRCh37.p13 chr5: 121,765,068-121,765,154 SNCAIP
    nsv6777565copy number variation1nstd229human GRCh38 chr5: 122,338,201-122,377,400 , GRCh37.p13 chr5: 121,673,896-121,713,095 SNCAIP, ANCV1RP
    nsv6777331copy number variation1nstd229human GRCh38 chr5: 122,321,468-122,327,048 , GRCh37.p13 chr5: 121,657,163-121,662,743 SNCAIP
    nsv6777307copy number variation1nstd229human GRCh38 chr5: 122,368,101-122,377,500 , GRCh37.p13 chr5: 121,703,796-121,713,195 ANCV1RP, SNCAIP
    nsv6777031copy number variation1nstd229human GRCh38 chr5: 122,342,736-122,342,896 , GRCh37.p13 chr5: 121,678,431-121,678,591 SNCAIP
    nsv6776823copy number variation1nstd229human GRCh38 chr5: 122,277,519-122,450,869 , GRCh37.p13 chr5: 121,613,214-121,786,564 MGC32805, ANCV1RP, 1 more genes
    nsv6776282copy number variation1nstd229human GRCh38 chr5: 122,339,801-122,377,600 , GRCh37.p13 chr5: 121,675,496-121,713,295 ANCV1RP, SNCAIP
    nsv6775465copy number variation1nstd229human GRCh38 chr5: 122,448,501-122,452,400 , GRCh37.p13 chr5: 121,784,196-121,788,095 MGC32805, SNCAIP
    nsv6775286copy number variation1nstd229human GRCh38 chr5: 122,337,801-122,377,200 , GRCh37.p13 chr5: 121,673,496-121,712,895 SNCAIP, ANCV1RP
    nsv6772619copy number variation1nstd229human GRCh38 chr5: 122,340,801-122,377,200 , GRCh37.p13 chr5: 121,676,496-121,712,895 ANCV1RP, SNCAIP
    nsv6770741copy number variation1nstd229human GRCh38 chr5: 122,365,701-122,377,500 , GRCh37.p13 chr5: 121,701,396-121,713,195 ANCV1RP, SNCAIP
    nsv6770301copy number variation1nstd229human GRCh38 chr5: 122,378,301-122,379,100 , GRCh37.p13 chr5: 121,713,996-121,714,795 SNCAIP
    nsv6767680copy number variation1nstd229human GRCh38 chr5: 122,314,101-122,377,600 , GRCh37.p13 chr5: 121,649,796-121,713,295 ANCV1RP, SNCAIP
    nsv6767651copy number variation1nstd229human GRCh38 chr5: 122,383,401-122,509,600 , GRCh37.p13 chr5: 121,719,096-121,845,295 LOC107986446, MGC32805, 1 more genes
    nsv6765527copy number variation1nstd229human GRCh38 chr5: 122,365,801-122,377,400 , GRCh37.p13 chr5: 121,701,496-121,713,095 ANCV1RP, SNCAIP
    nsv6765510copy number variation1nstd229human GRCh38 chr5: 122,360,201-122,377,600 , GRCh37.p13 chr5: 121,695,896-121,713,295 ANCV1RP, SNCAIP
    nsv6764643copy number variation1nstd229human GRCh38 chr5: 122,378,401-122,379,000 , GRCh37.p13 chr5: 121,714,096-121,714,695 SNCAIP
    nsv6764365copy number variation1nstd229human GRCh38 chr5: 122,370,101-122,400,300 , GRCh37.p13 chr5: 121,705,796-121,735,995 ANCV1RP, SNCAIP
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