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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673729copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976 SEMA3B-AS1, GNAT1, 87 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5201436copy number variation1nstd204human GRCh37.p13 chr3: 49,439,734-49,516,233 , GRCh38.p13 chr3: 49,402,301-49,478,800 AMT, RHOA, 4 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
    nsv4914320copy number variation1nstd200human GRCh38 chr3: 49,398,014-49,478,066 , GRCh37.p13 chr3: 49,435,447-49,515,499 RNA5SP130, TCTA, 4 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
    nsv4728146copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,807,193-51,363,558 , GRCh38.p12 chr3: 48,769,760-51,326,127 APEH, MIR5193, 90 more genes
    nsv4683411copy number variation1nstd102humanPathogenic GRCh37 chr3: 49,158,649-49,570,642 , GRCh38.p12 chr3: 49,121,216-49,533,209 C3orf84, RHOA, 15 more genes
    nsv4683080copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 49,457,133-49,457,231 , GRCh38.p12 chr3: 49,419,700-49,419,798 AMT
    nsv4682682copy number variation1nstd102humanPathogenic GRCh37 chr3: 49,458,915-49,461,781 , GRCh38.p12 chr3: 49,421,482-49,424,348 NICN1, AMT
    nsv4674083copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,346,677-49,630,228 , GRCh38.p12 chr3: 48,305,187-49,592,795 MIR6823, NCKIPSD, 59 more genes
    nsv4596501copy number variation1nstd183human GRCh37 chr3: 49,448,793-49,454,610 , GRCh38.p12 chr3: 49,411,360-49,417,177 AMT, TCTA, 1 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
    nsv4381849copy number variation1nstd173human GRCh37 chr3: 49,409,382-49,474,392 , GRCh38.p12 chr3: 49,371,949-49,436,959 NICN1, TCTA, 2 more genes
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 UQCRC1, DHX30, 291 more genes
    nsv4342799sequence alteration1nstd166human GRCh37.p13 chr3: 49,363,693-49,487,596 , GRCh38.p12 chr3: 49,326,260-49,450,163 AMT, RHOA, 4 more genes
    nsv4077970copy number variation1nstd166human GRCh37.p13 chr3: 49,448,000-49,453,500 , GRCh38.p12 chr3: 49,410,567-49,416,067 TCTA, RHOA, 1 more genes
    nsv3921797copy number variation1nstd102humanPathogenic NCBI36 chr3: 45,896,379-50,762,357 , GRCh38 chr3: 45,879,883-50,749,922 , GRCh37 chr3: 45,921,375-50,787,353 RBM5-AS1, PRSS42P, 185 more genes
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