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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130913insertion1nstd186human GRCh37 chr19: 44,052,209-44,052,217 , GRCh38.p12 chr19: 43,548,057-43,548,065 XRCC1
    nsv5975431insertion1nstd209human GRCh38 chr19: 43,548,049-43,548,049 , GRCh37.p13 chr19: 44,052,201-44,052,201 XRCC1
    nsv5727977mobile element insertion2nstd211human GRCh38 chr19: 43,559,931-43,559,931 , GRCh37.p13 chr19: 44,064,083-44,064,083 XRCC1
    nsv5657664insertion1nstd207human GRCh38 chr19: 43,548,049-43,548,049 , GRCh37.p13 chr19: 44,052,201-44,052,201 XRCC1
    nsv5657191insertion1nstd207human GRCh38 chr19: 43,559,097-43,559,097 , GRCh37.p13 chr19: 44,063,249-44,063,249 XRCC1
    nsv5542484insertion1nstd206human GRCh38 chr19: 43,548,057-43,548,065 , GRCh37.p13 chr19: 44,052,209-44,052,217 XRCC1
    nsv5528713copy number variation1nstd206human GRCh38 chr19: 43,559,077-43,559,473 , GRCh37.p13 chr19: 44,063,229-44,063,625 XRCC1
    nsv5326450copy number variation1nstd204human GRCh38.p13 chr19: 43,559,261-43,560,142 , GRCh37.p13 chr19: 44,063,413-44,064,294 XRCC1
    nsv5193553mobile element insertion1nstd203human GRCh38 chr19: 43,559,916-43,559,930 , GRCh37.p13 chr19: 44,064,068-44,064,082 XRCC1
    nsv5024672copy number variation1nstd200human GRCh38 chr19: 42,797,406-43,578,600 , GRCh37.p13 chr19: 43,301,558-44,082,752 , PINLYP, 28 more genes
    nsv5020596copy number variation1nstd200human GRCh38 chr19: 43,569,180-43,569,430 , GRCh37.p13 chr19: 44,073,332-44,073,582 XRCC1
    nsv5020595copy number variation1nstd200human GRCh38 chr19: 43,566,333-43,566,476 , GRCh37.p13 chr19: 44,070,485-44,070,628 XRCC1
    nsv4868504copy number variation1nstd200human GRCh37 chr19: 44,063,454-44,064,301 , GRCh38.p12 chr19: 43,559,302-43,560,149 XRCC1
    nsv4757925insertion1nstd199human GRCh37 chr19: 44,052,210-44,052,210 , GRCh38.p12 chr19: 43,548,058-43,548,058 XRCC1
    nsv4679272copy number variation1nstd189human GRCh37.p13 chr19: 43,906,705-44,198,705 , GRCh38.p12 chr19: 43,402,553-43,694,553 , PLAUR, 16 more genes
    nsv4631886copy number variation1nstd183human GRCh37 chr19: 43,959,697-44,055,058 , GRCh38.p12 chr19: 43,455,545-43,550,906 XRCC1, ETHE1, 3 more genes
    nsv4573991mobile element insertion1nstd166human GRCh37.p13 chr19: 44,064,068-44,064,068 , GRCh38.p12 chr19: 43,559,916-43,559,916 XRCC1
    nsv4457468copy number variation1nstd102humanUncertain significance GRCh37 chr19: 43,818,072-44,100,076 , GRCh38.p12 chr19: 43,313,920-43,595,924 CD177, LYPD3, 11 more genes
    nsv4457412copy number variation1nstd102humanUncertain significance GRCh37 chr19: 43,803,157-44,105,375 , GRCh38.p12 chr19: 43,299,005-43,601,223 ZNF575, CEACAMP4, 12 more genes
    nsv4457378copy number variation1nstd102humanUncertain significance GRCh37 chr19: 44,004,424-44,080,746 , GRCh38.p12 chr19: 43,500,272-43,576,594 ETHE1, PHLDB3, 3 more genes
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