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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074360inversion1nstd229human GRCh38 chr9: 122,316,047-122,316,129 , GRCh37.p13 chr9: 125,078,326-125,078,408 MRRF
    nsv6875574copy number variation1nstd229human GRCh38 chr9: 122,312,869-122,313,011 , GRCh37.p13 chr9: 125,075,148-125,075,290 MRRF
    nsv6871225copy number variation1nstd229human GRCh38 chr9: 122,326,514-122,326,598 , GRCh37.p13 chr9: 125,088,793-125,088,877 MRRF
    nsv6870065copy number variation1nstd229human GRCh38 chr9: 122,284,233-122,296,271 , GRCh37.p13 chr9: 125,046,512-125,058,550 MRRF
    nsv6866700copy number variation1nstd229human GRCh38 chr9: 122,278,296-122,281,165 , GRCh37.p13 chr9: 125,040,575-125,043,444 MRRF
    nsv6862485copy number variation1nstd229human GRCh38 chr9: 122,318,889-122,318,929 , GRCh37.p13 chr9: 125,081,168-125,081,208 MRRF
    nsv6862045copy number variation1nstd229human GRCh38 chr9: 122,277,601-122,286,300 , GRCh37.p13 chr9: 125,039,880-125,048,579 MRRF
    nsv6861039copy number variation1nstd229human GRCh38 chr9: 122,322,501-122,326,400 , GRCh37.p13 chr9: 125,084,780-125,088,679 MRRF
    nsv6859120copy number variation1nstd229human GRCh38 chr9: 122,268,176-122,377,242 , GRCh37.p13 chr9: 125,030,455-125,139,521 MRRF, PTGS1
    nsv6637981copy number variation1nstd102humanPathogenic GRCh37 chr9: 124,018,736-129,995,568 , GRCh38.p12 chr9: 121,256,458-127,233,289 PBX3-DT, ADGRD2, 119 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6439357copy number variation1nstd223human GRCh38 chr9: 122,322,481-122,326,449 , GRCh37.p13 chr9: 125,084,760-125,088,728 MRRF
    nsv6436334copy number variation1nstd223human GRCh38 chr9: 122,257,235-122,276,075 , GRCh37.p13 chr9: 125,019,514-125,038,354 RBM18, MRRF
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6308856mobile element insertion1nstd186human GRCh37 chr9: 125,049,862-125,049,913 , GRCh38.p12 chr9: 122,287,583-122,287,634 MRRF
    nsv6291398copy number variation1nstd102humanPathogenic GRCh37 chr9: 120,045,175-127,335,905 , GRCh38.p12 chr9: 117,282,896-124,573,626 ZBTB6, LOC105376253, 107 more genes
    nsv6137052copy number variation1nstd213human GRCh37 chr9: 123,200,000-125,840,001 , GRCh38.p12 chr9: 120,437,722-123,077,722 MEGF9, GGTA1, 61 more genes
    nsv6089703insertion1nstd212human GRCh38 chr9: 122,324,307-122,324,307 , GRCh37.p13 chr9: 125,086,586-125,086,586 MRRF
    nsv6085373insertion1nstd212human GRCh38 chr9: 122,272,623-122,272,623 , GRCh37.p13 chr9: 125,034,902-125,034,902 MRRF
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