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Items: 1 to 20 of 1115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5976235inversion1nstd209human GRCh38 chr10: 133,450,717-133,466,983 , GRCh37.p13 chr10: 135,264,221-135,280,487 , SCART1
    nsv5976116insertion1nstd209human GRCh38 chr10: 133,460,497-133,460,497 , GRCh37.p13 chr10: 135,274,001-135,274,001 , SCART1
    nsv5926289copy number variation1nstd209human GRCh38 chr10: 133,371,188-133,471,140 , GRCh37.p13 chr10: 135,184,692-135,284,644 , ECHS1, 6 more genes
    nsv5922312copy number variation1nstd209human GRCh38 chr10: 133,459,648-133,466,814 , GRCh37.p13 chr10: 135,273,152-135,280,318 , SCART1
    nsv5860641copy number variation1nstd209human GRCh38 chr10: 133,450,137-133,462,726 , GRCh37.p13 chr10: 135,263,641-135,276,230 , SCART1
    nsv5849562copy number variation1nstd209human GRCh38 chr10: 133,460,604-133,463,126 , GRCh37.p13 chr10: 135,274,108-135,276,630 , SCART1
    nsv5672526copy number variation1nstd102humanPathogenic GRCh37 chr10: 127,548,166-135,440,251 , GRCh38.p12 chr10: 125,859,597-133,626,747 LINC00601, RPL5P28, 110 more genes
    nsv5659660insertion1nstd207human GRCh38 chr10: 133,460,509-133,460,509 , GRCh37.p13 chr10: 135,274,013-135,274,013 , SCART1
    nsv5652600insertion1nstd207human GRCh38 chr10: 133,454,158-133,454,158 , GRCh37.p13 chr10: 135,267,662-135,267,662 SCART1
    nsv5646957insertion1nstd207human GRCh38 chr10: 133,464,312-133,464,312 , GRCh37.p13 chr10: 135,277,816-135,277,816 , SCART1
    nsv5505886copy number variation1nstd206human GRCh38 chr10: 133,426,565-133,573,130 , GRCh37.p13 chr10: 135,240,069-135,386,634 , SPRNP1, 8 more genes
    nsv5501586copy number variation1nstd206human GRCh38 chr10: 133,401,130-133,457,130 , GRCh37.p13 chr10: 135,214,634-135,270,634 MTG1, SCART1, 2 more genes
    nsv5498623copy number variation1nstd206human GRCh38 chr10: 133,465,680-133,465,779 , GRCh37.p13 chr10: 135,279,184-135,279,283 SCART1
    nsv5497654copy number variation1nstd206human GRCh38 chr10: 133,454,158-133,454,330 , GRCh37.p13 chr10: 135,267,662-135,267,834 SCART1
    nsv5381769copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,483,682-135,434,178 , GRCh38.p12 chr10: 127,685,418-133,620,674 DPYSL4, LINC02667, 88 more genes
    nsv5335748translocation1nstd200human GRCh37 chr10: 135,198,056-135,198,056 , GRCh37 chr10: 135,272,867-135,272,867 , GRCh38.p12 chr10: 133,459,363-133,459,363 , GRCh38.p12 chr10: 133,384,552-133,384,552 SCART1, PAOX
    nsv5254134copy number variation1nstd204human GRCh38.p13 chr10: 133,436,976-133,456,586 , GRCh37.p13 chr10: 135,250,480-135,270,090 SCART1
    nsv5250511copy number variation1nstd204human GRCh37.p13 chr10: 135,247,805-135,351,304 , GRCh38.p13 chr10: 133,434,301-133,537,800 , CYP2E1, 4 more genes
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