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Items: 1 to 20 of 289

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945205copy number variation1nstd209human GRCh38 chr19: 45,580,260-45,580,881 , GRCh37.p13 chr19: 46,083,518-46,084,139 OPA3
    nsv5929979copy number variation1nstd209human GRCh38 chr19: 45,566,180-45,566,501 , GRCh37.p13 chr19: 46,069,438-46,069,759 OPA3
    nsv5929540copy number variation1nstd209human GRCh38 chr19: 45,533,041-45,534,781 , GRCh37.p13 chr19: 46,036,299-46,038,039 OPA3
    nsv5927556copy number variation1nstd209human GRCh38 chr19: 45,572,308-45,572,393 , GRCh37.p13 chr19: 46,075,566-46,075,651 OPA3
    nsv5882882copy number variation1nstd209human GRCh38 chr19: 45,570,005-45,571,104 , GRCh37.p13 chr19: 46,073,263-46,074,362 OPA3
    nsv5870078copy number variation1nstd209human GRCh38 chr19: 45,533,344-45,534,874 , GRCh37.p13 chr19: 46,036,602-46,038,132 OPA3
    nsv5723717mobile element insertion1nstd211human GRCh38 chr19: 45,550,197-45,550,197 , GRCh37.p13 chr19: 46,053,455-46,053,455 OPA3
    nsv5673225copy number variation1nstd102humanUncertain significance GRCh37 chr19: 46,057,054-46,057,106 , GRCh38 chr19: 45,553,796-45,553,848 OPA3
    nsv5595546copy number variation1nstd207human GRCh38 chr19: 45,572,280-45,572,361 , GRCh37.p13 chr19: 46,075,538-46,075,619 OPA3
    nsv5555882sequence alteration1nstd206human GRCh38 chr19: 45,580,124-46,272,839 , GRCh37.p13 chr19: 46,083,382-46,776,096 , SYMPK, 39 more genes
    nsv5532659copy number variation1nstd206human GRCh38 chr19: 45,533,041-45,534,782 , GRCh37.p13 chr19: 46,036,299-46,038,040 OPA3
    nsv5526172copy number variation1nstd206human GRCh38 chr19: 45,572,116-45,572,525 , GRCh37.p13 chr19: 46,075,374-46,075,783 OPA3
    nsv5517487copy number variation1nstd206human GRCh38 chr19: 45,581,689-45,581,768 , GRCh37.p13 chr19: 46,084,947-46,085,026 OPA3
    nsv5375463translocation1nstd200human GRCh38 chr19: 45,533,082-45,533,082 , GRCh38 chr19: 45,534,733-45,534,733 , GRCh37.p13 chr19: 46,036,340-46,036,340 , GRCh37.p13 chr19: 46,037,991-46,037,991 OPA3
    nsv5359843translocation1nstd200human GRCh38 chr19: 45,551,409-45,551,409 , GRCh38 chr19: 45,551,483-45,551,483 , GRCh37.p13 chr19: 46,054,741-46,054,741 , GRCh37.p13 chr19: 46,054,667-46,054,667 OPA3
    nsv5327341copy number variation1nstd204human GRCh38.p13 chr19: 45,584,936-45,884,300 , GRCh37.p13 chr19: 46,088,194-46,387,558 DMWD, GPR4, 19 more genes
    nsv5320545copy number variation1nstd204human GRCh38.p13 chr19: 45,579,389-45,580,156 , GRCh37.p13 chr19: 46,082,647-46,083,414 OPA3
    nsv5297987copy number variation1nstd204human GRCh38.p13 chr19: 45,572,301-45,648,300 , GRCh37.p13 chr19: 46,075,559-46,151,558 OPA3, EML2-AS1, 3 more genes
    nsv5285123copy number variation1nstd204human GRCh37.p13 chr19: 45,992,859-46,051,858 , GRCh38.p13 chr19: 45,489,601-45,548,600 RTN2, VASP, 4 more genes
    nsv5284788copy number variation1nstd204human GRCh38.p13 chr19: 45,504,601-45,776,400 , GRCh37.p13 chr19: 46,007,859-46,279,658 MIR642A, LOC107985315, 17 more genes
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