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Items: 1 to 20 of 99

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048850inversion1nstd229human GRCh38 chr3: 37,408,411-39,634,596 , GRCh37.p13 chr3: 37,449,902-39,676,087 OXSR1, ITGA9, 55 more genes
    nsv6716195copy number variation1nstd229human GRCh38 chr3: 39,359,969-39,382,103 , GRCh37.p13 chr3: 39,401,460-39,423,594 LOC105377037, LOC105377644, 2 more genes
    nsv6711902copy number variation1nstd229human GRCh38 chr3: 38,527,947-43,061,183 , GRCh37.p13 chr3: 38,569,438-43,102,675 ZBTB47, VIPR1-AS1, 90 more genes
    nsv6705109copy number variation1nstd229human GRCh38 chr3: 39,362,301-39,416,000 , GRCh37.p13 chr3: 39,403,792-39,457,491 SNORA6, LOC105377037, 4 more genes
    nsv6543288inversion1nstd223human GRCh38 chr3: 39,393,099-39,393,664 , GRCh37.p13 chr3: 39,434,590-39,435,155 SLC25A38
    nsv6537958inversion1nstd223human GRCh38 chr3: 37,408,438-39,634,613 , GRCh37.p13 chr3: 37,449,929-39,676,104 ITGA9-AS1, MIR26A1, 55 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv5898340copy number variation1nstd209human GRCh38 chr3: 39,394,123-39,394,297 , GRCh37.p13 chr3: 39,435,614-39,435,788 SLC25A38
    nsv5893972copy number variation1nstd209human GRCh38 chr3: 39,388,703-39,389,188 , GRCh37.p13 chr3: 39,430,194-39,430,679 SLC25A38
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4910882copy number variation1nstd200human GRCh38 chr3: 39,390,206-39,390,284 , GRCh37.p13 chr3: 39,431,697-39,431,775 SLC25A38
    nsv4910881copy number variation1nstd200human GRCh38 chr3: 39,384,712-39,384,982 , GRCh37.p13 chr3: 39,426,203-39,426,473 SLC25A38
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4806645copy number variation1nstd200human GRCh37 chr3: 39,430,196-39,430,680 , GRCh38.p12 chr3: 39,388,705-39,389,189 SLC25A38
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4471331mobile element insertion1nstd166human GRCh37.p13 chr3: 39,437,775-39,437,775 , GRCh38.p12 chr3: 39,396,284-39,396,284 SLC25A38
    nsv4471330mobile element insertion1nstd166human GRCh37.p13 chr3: 39,424,611-39,424,611 , GRCh38.p12 chr3: 39,383,120-39,383,120 SLC25A38, LOC105377644
    nsv3917642copy number variation1nstd102humanPathogenic NCBI36 chr3: 33,744,902-40,678,946 , GRCh37 chr3: 33,769,898-40,703,942 , GRCh38 chr3: 33,728,406-40,662,451 STAC, SCN11A, 111 more genes
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