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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947088copy number variation1nstd209human GRCh38 chr19: 41,803,755-41,807,379 , GRCh37.p13 chr19|NW_004775434.1: 372,794-376,418 , GRCh37.p13 chr19: 42,307,802-42,311,244 CEACAM3, LOC100422623
    nsv5938284copy number variation1nstd209human GRCh38 chr19: 41,803,700-41,807,212 , GRCh37.p13 chr19: 42,307,802-42,311,244 , GRCh37.p13 chr19|NW_004775434.1: 372,739-376,251 LOC100422623, CEACAM3
    nsv5705557mobile element insertion2nstd211human GRCh38 chr19: 41,807,206-41,807,206 , GRCh37.p13 chr19: 42,311,244-42,311,244 , GRCh37.p13 chr19|NW_004775434.1: 376,245-376,245 CEACAM3, LOC100422623
    nsv5697537mobile element insertion2nstd211human GRCh38 chr19: 41,799,481-41,799,481 , GRCh37.p13 chr19: 42,303,413-42,303,413 , GRCh37.p13 chr19|NW_004775434.1: 368,520-368,520 CEACAM3
    nsv5648221insertion1nstd207human GRCh38 chr19: 41,803,704-41,803,704 , GRCh37.p13 chr19|NW_004775434.1: 372,743-372,743 CEACAM3
    nsv5562413sequence alteration1nstd206human GRCh38 chr19: 41,797,706-42,527,281 , GRCh37.p13 chr19: 42,514,712-43,031,433 MEGF8, LIPE, 34 more genes
    nsv5558687sequence alteration1nstd206human GRCh38 chr19: 41,803,700-41,803,755 , GRCh37.p13 chr19|NW_004775434.1: 372,739-372,794 CEACAM3
    nsv5554149sequence alteration1nstd206human GRCh38 chr19: 41,749,279-42,444,786 , GRCh37.p13 chr19: 42,514,712-42,948,938 ERF, CEACAM6, 32 more genes
    nsv5550933insertion1nstd206human GRCh38 chr19: 41,803,700-41,803,700 , GRCh37.p13 chr19|NW_004775434.1: 372,739-372,739 CEACAM3
    nsv5531627copy number variation1nstd206human GRCh38 chr19: 41,806,271-41,816,663 , GRCh37.p13 chr19: 42,310,312-42,320,699 , GRCh37.p13 chr19|NW_004775434.1: 375,310-385,702 CEACAM3, LOC100422623
    nsv5416721mobile element insertion1nstd206human GRCh38 chr19: 41,799,481-41,799,532 , GRCh37.p13 chr19|NW_004775434.1: 368,520-368,571 , GRCh37.p13 chr19: 42,303,413-42,303,464 CEACAM3
    nsv5365854translocation1nstd200human GRCh38 chr19: 41,803,755-41,803,755 , GRCh38 chr19: 41,807,383-41,807,383 , GRCh37.p13 chr19|NW_004775434.1: 376,422-376,422 , GRCh37.p13 chr19|NW_004775434.1: 372,794-372,794 CEACAM3, LOC100422623
    nsv5359811translocation1nstd200human GRCh38 chr19: 41,807,206-41,807,206 , GRCh38 chr19: 41,803,700-41,803,700 , GRCh37.p13 chr19|NW_004775434.1: 376,245-376,245 , GRCh37.p13 chr19|NW_004775434.1: 372,739-372,739 , GRCh37.p13 chr19: 42,311,244-42,311,244 CEACAM3, LOC100422623
    nsv5327720translocation1nstd204human GRCh37.p13 chr19|NW_004775434.1: 376,422-376,422 , GRCh37.p13 chr19|NW_004775434.1: 372,794-372,794 , GRCh38.p13 chr19: 41,803,755-41,803,755 , GRCh38.p13 chr19: 41,807,383-41,807,383 CEACAM3, LOC100422623
    nsv5326470translocation1nstd204human GRCh37.p13 chr19|NW_004775434.1: 376,245-376,245 , GRCh37.p13 chr19|NW_004775434.1: 372,739-372,739 , GRCh37.p13 chr19: 42,311,244-42,311,244 , GRCh38.p13 chr19: 41,803,700-41,803,700 , GRCh38.p13 chr19: 41,807,206-41,807,206 CEACAM3, LOC100422623
    nsv5175542mobile element insertion1nstd203human GRCh38 chr19: 41,807,213-41,807,213 , GRCh37.p13 chr19|NW_004775434.1: 376,252-376,252 CEACAM3, LOC100422623
    nsv5174370mobile element insertion1nstd203human GRCh38 chr19: 41,807,204-41,807,204 , GRCh37.p13 chr19|NW_004775434.1: 376,243-376,243 , GRCh37.p13 chr19: 42,311,242-42,311,242 LOC100422623, CEACAM3
    nsv5170329mobile element insertion1nstd203human GRCh38 chr19: 41,807,209-41,807,209 , GRCh37.p13 chr19|NW_004775434.1: 376,248-376,248 CEACAM3, LOC100422623
    nsv5161983mobile element insertion1nstd203human GRCh38 chr19: 41,807,206-41,807,206 , GRCh37.p13 chr19|NW_004775434.1: 376,245-376,245 , GRCh37.p13 chr19: 42,311,244-42,311,244 CEACAM3, LOC100422623
    nsv5024658copy number variation1nstd200human GRCh38 chr19: 41,756,999-41,884,097 , GRCh37.p13 chr19: 42,260,907-42,388,164 , GRCh37.p13 chr19|NW_004775434.1: 326,038-453,136 ARHGEF1, DMRTC2, 9 more genes
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