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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097206copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,109,903-53,164,416 , GRCh38.p12 chr3: 52,075,887-53,130,400 PHF7, SEMA3G, 47 more genes
    nsv7096813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406 DNAH1, BAP1, 62 more genes
    nsv7055197inversion1nstd229human GRCh38 chr3: 52,426,847-52,608,000 , GRCh37.p13 chr3: 52,460,863-52,642,016 STAB1, PBRM1, 7 more genes
    nsv7041270inversion1nstd229human GRCh38 chr3: 52,619,221-53,173,329 , GRCh37.p13 chr3: 52,653,237-53,185,061 SNORD19, SNORD19C, 23 more genes
    nsv6717956copy number variation1nstd229human GRCh38 chr3: 52,650,204-52,702,405 , GRCh37.p13 chr3: 52,684,220-52,736,421 SNORD19B, GLT8D1, 6 more genes
    nsv6716874copy number variation1nstd229human GRCh38 chr3: 52,619,220-52,838,314 , GRCh37.p13 chr3: 52,653,236-52,872,330 ITIH4-AS1, STIMATE, 18 more genes
    nsv6716684copy number variation1nstd229human GRCh38 chr3: 52,630,603-52,630,808 , GRCh37.p13 chr3: 52,664,619-52,664,824 PBRM1
    nsv6716085copy number variation1nstd229human GRCh38 chr3: 52,604,908-52,608,000 , GRCh37.p13 chr3: 52,638,924-52,642,016 PBRM1
    nsv6715600copy number variation1nstd229human GRCh38 chr3: 52,628,201-52,691,600 , GRCh37.p13 chr3: 52,662,217-52,725,616 SNORD19C, SNORD19, 5 more genes
    nsv6715302copy number variation1nstd229human GRCh38 chr3: 52,656,401-52,872,900 , GRCh37.p13 chr3: 52,690,417-52,906,916 SNORD136, GLT8D1, 19 more genes
    nsv6713675copy number variation1nstd229human GRCh38 chr3: 52,547,701-52,692,100 , GRCh37.p13 chr3: 52,581,717-52,726,116 SNORD19B, SNORD136, 7 more genes
    nsv6711180copy number variation1nstd229human GRCh38 chr3: 52,600,605-52,601,272 , GRCh37.p13 chr3: 52,634,621-52,635,288 PBRM1
    nsv6709114copy number variation1nstd229human GRCh38 chr3: 52,571,095-52,571,126 , GRCh37.p13 chr3: 52,605,111-52,605,142 PBRM1
    nsv6707715copy number variation1nstd229human GRCh38 chr3: 52,681,958-52,682,323 , GRCh37.p13 chr3: 52,715,974-52,716,339 PBRM1
    nsv6706182copy number variation1nstd229human GRCh38 chr3: 52,596,807-52,600,132 , GRCh37.p13 chr3: 52,630,823-52,634,148 PBRM1
    nsv6702571copy number variation1nstd229human GRCh38 chr3: 52,581,987-52,584,277 , GRCh37.p13 chr3: 52,616,003-52,618,293 PBRM1
    nsv6702443copy number variation1nstd229human GRCh38 chr3: 52,572,731-52,574,842 , GRCh37.p13 chr3: 52,606,747-52,608,858 PBRM1
    nsv6700933copy number variation1nstd229human GRCh38 chr3: 52,548,501-52,550,200 , GRCh37.p13 chr3: 52,582,517-52,584,216 RNU6-856P, PBRM1
    nsv6699647copy number variation1nstd229human GRCh38 chr3: 52,675,833-52,676,156 , GRCh37.p13 chr3: 52,709,849-52,710,172 PBRM1
    nsv6555197inversion1nstd223human GRCh38 chr3: 52,643,804-52,644,696 , GRCh37.p13 chr3: 52,677,820-52,678,712 PBRM1
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