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Items: 1 to 20 of 426

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096952copy number variation3nstd102humanUncertain significance GRCh37 chr3: 188,118,572-192,126,012 , GRCh38.p12 chr3: 188,400,784-192,408,223 P3H2, GMNC, 39 more genes
    nsv7096556copy number variation1nstd102humanUncertain significance GRCh37 chr3: 189,455,509-192,126,012 , GRCh38.p12 chr3: 189,737,720-192,408,223 LOC107986171, OSTN, 30 more genes
    nsv7054565inversion1nstd229human GRCh38 chr3: 190,576,537-190,578,454 , GRCh37.p13 chr3: 190,294,326-190,296,243 IL1RAP
    nsv7040429inversion1nstd229human GRCh38 chr3: 184,379,670-192,292,047 , GRCh37.p13 chr3: 184,097,458-192,009,836 LOC107986163, RPL34P10, 123 more genes
    nsv6736903copy number variation1nstd229human GRCh38 chr3: 190,626,195-190,634,903 , GRCh37.p13 chr3: 190,343,984-190,352,692 IL1RAP
    nsv6735820copy number variation1nstd229human GRCh38 chr3: 190,496,366-190,516,685 , GRCh37.p13 chr3: 190,214,155-190,234,474 IL1RAP
    nsv6735271copy number variation1nstd229human GRCh38 chr3: 190,580,671-190,593,126 , GRCh37.p13 chr3: 190,298,460-190,310,915 IL1RAP
    nsv6733546copy number variation1nstd229human GRCh38 chr3: 190,524,281-190,531,773 , GRCh37.p13 chr3: 190,242,070-190,249,562 IL1RAP
    nsv6733518copy number variation1nstd229human GRCh38 chr3: 189,977,007-192,427,323 , GRCh37.p13 chr3: 189,694,796-192,145,112 RN7SKP296, LOC105374277, 27 more genes
    nsv6732846copy number variation1nstd229human GRCh38 chr3: 190,526,842-190,531,333 , GRCh37.p13 chr3: 190,244,631-190,249,122 IL1RAP
    nsv6732193copy number variation1nstd229human GRCh38 chr3: 190,618,702-191,189,943 , GRCh37.p13 chr3: 190,336,491-190,907,732 IL1RAP, GMNC, 7 more genes
    nsv6730690copy number variation1nstd229human GRCh38 chr3: 190,586,790-190,586,829 , GRCh37.p13 chr3: 190,304,579-190,304,618 IL1RAP
    nsv6730560copy number variation1nstd229human GRCh38 chr3: 190,572,861-190,573,147 , GRCh37.p13 chr3: 190,290,650-190,290,936 IL1RAP
    nsv6729012copy number variation1nstd229human GRCh38 chr3: 190,654,080-190,660,735 , GRCh37.p13 chr3: 190,371,869-190,378,524 IL1RAP
    nsv6724812copy number variation1nstd229human GRCh38 chr3: 190,631,482-190,635,072 , GRCh37.p13 chr3: 190,349,271-190,352,861 IL1RAP
    nsv6723748copy number variation1nstd229human GRCh38 chr3: 190,621,819-190,621,922 , GRCh37.p13 chr3: 190,339,608-190,339,711 IL1RAP
    nsv6723630copy number variation1nstd229human GRCh38 chr3: 190,657,017-190,988,806 , GRCh37.p13 chr3: 190,374,806-190,706,595 GMNC, CCT6P4, 4 more genes
    nsv6723515copy number variation1nstd229human GRCh38 chr3: 190,591,343-190,598,355 , GRCh37.p13 chr3: 190,309,132-190,316,144 IL1RAP
    nsv6723334copy number variation1nstd229human GRCh38 chr3: 190,631,907-190,632,044 , GRCh37.p13 chr3: 190,349,696-190,349,833 IL1RAP
    nsv6722538copy number variation1nstd229human GRCh38 chr3: 190,459,055-190,718,744 , GRCh37.p13 chr3: 190,176,844-190,436,533 IL1RAP, RN7SKP296, 3 more genes
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