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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053396inversion1nstd229human GRCh38 chr3: 25,039,226-25,464,038 , GRCh37.p13 chr3: 25,080,717-25,505,529 RNA5SP126, H3P10, 3 more genes
    nsv6717031copy number variation1nstd229human GRCh38 chr3: 25,329,936-25,399,509 , GRCh37.p13 chr3: 25,371,427-25,441,000 RARB, RARB-AS1, 1 more genes
    nsv6715501copy number variation1nstd229human GRCh38 chr3: 24,933,260-25,871,078 , GRCh37.p13 chr3: 24,974,751-25,912,569 CRIP1P2, MIR4442, 14 more genes
    nsv6713157copy number variation1nstd229human GRCh38 chr3: 25,337,532-25,373,798 , GRCh37.p13 chr3: 25,379,023-25,415,289 RNA5SP126, RARB
    nsv6710277copy number variation1nstd229human GRCh38 chr3: 25,251,139-25,383,689 , GRCh37.p13 chr3: 25,292,630-25,425,180 RNA5SP126, RARB, 2 more genes
    nsv6362861copy number variation1nstd223human GRCh38 chr3: 25,352,801-25,356,600 , GRCh37.p13 chr3: 25,394,292-25,398,091 RNA5SP126, RARB
    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
    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
    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
    nsv4674775copy number variation1nstd102humanUncertain significance GRCh37 chr3: 25,319,259-25,713,461 , GRCh38.p12 chr3: 25,277,768-25,671,970 MIR4442, CFL1P7, 5 more genes
    nsv4673920copy number variation1nstd102humanUncertain significance GRCh37 chr3: 25,329,791-25,554,978 , GRCh38.p12 chr3: 25,288,300-25,513,487 RARB, H3P10, 3 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4452346copy number variation1nstd102humanPathogenic GRCh37 chr3: 19,064,852-26,448,689 , GRCh38.p12 chr3: 19,023,360-26,407,198 RPL15, SGO1, 71 more genes
    nsv4073361copy number variation1nstd166human GRCh37.p13 chr3: 25,361,689-25,394,756 , GRCh38.p12 chr3: 25,320,198-25,353,265 CFL1P7, RARB, 1 more genes
    nsv3923656copy number variation1nstd102humanPathogenic GRCh38 chr3: 11,463,328-38,919,543 , NCBI36 chr3: 11,479,802-38,936,038 , GRCh37 chr3: 11,504,802-38,961,034 RN7SL4P, TOP2B, 348 more genes
    nsv3923353copy number variation1nstd102humanPathogenic GRCh38 chr3: 19,915,382-25,537,973 , GRCh37 chr3: 19,956,874-25,579,464 , NCBI36 chr3: 19,931,878-25,554,468 RNU6-822P, UBE2E1-AS1, 52 more genes
    nsv3912677copy number variation1nstd102humanUncertain significance NCBI36 chr3: 24,904,599-25,456,180 , GRCh37 chr3: 24,929,595-25,481,176 , GRCh38 chr3: 24,888,104-25,439,685 RARB, RNA5SP125, 5 more genes
    nsv3905127copy number variation1nstd102humanPathogenic GRCh37 chr3: 94,991-41,423,012 , NCBI36 chr3: 69,991-41,398,016 , GRCh38 chr3: 53,308-41,381,521 LINC02022, RPL23AP43, 540 more genes
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