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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921196copy number variation1nstd209human GRCh38 chr9: 104,132,666-104,133,854 , GRCh37.p13 chr9: 106,894,947-106,896,135 SMC2
    nsv5919487copy number variation1nstd209human GRCh38 chr9: 104,139,878-104,139,931 , GRCh37.p13 chr9: 106,902,159-106,902,212 SMC2
    nsv5708246mobile element insertion1nstd211human GRCh38 chr9: 104,110,809-104,110,809 , GRCh37.p13 chr9: 106,873,090-106,873,090 SMC2
    nsv5540041insertion1nstd206human GRCh38 chr9: 104,114,598-104,114,649 , GRCh37.p13 chr9: 106,876,879-106,876,930 SMC2
    nsv5489859copy number variation1nstd206human GRCh38 chr9: 104,124,293-104,124,375 , GRCh37.p13 chr9: 106,886,574-106,886,656 SMC2
    nsv5399043mobile element insertion1nstd206human GRCh38 chr9: 104,110,809-104,110,860 , GRCh37.p13 chr9: 106,873,090-106,873,141 SMC2
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5378342translocation1nstd200human GRCh38 chr9: 104,126,456-104,126,456 , GRCh38 chr6: 29,952,848-29,952,848 , GRCh37.p13 chr9: 106,888,737-106,888,737 , GRCh37.p13 chr6: 29,920,625-29,920,625 SMC2
    nsv5253970copy number variation1nstd204human GRCh38.p13 chr9: 104,126,036-104,127,435 , GRCh37.p13 chr9: 106,888,317-106,889,716 SMC2
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4982944copy number variation1nstd200human GRCh38 chr9: 104,122,013-104,122,189 , GRCh37.p13 chr9: 106,884,294-106,884,470 SMC2
    nsv4982943copy number variation1nstd200human GRCh38 chr9: 104,085,388-104,221,145 , GRCh37.p13 chr9: 106,847,669-106,983,426 SMC2-DT, SMC2
    nsv4831743copy number variation1nstd200human GRCh37 chr9: 106,847,669-106,983,426 , GRCh38.p12 chr9: 104,085,388-104,221,145 SMC2-DT, SMC2
    nsv4729415copy number variation1nstd102humanUncertain significance GRCh37 chr9: 106,846,395-106,986,277 , GRCh38.p12 chr9: 104,084,114-104,223,996 SMC2-DT, SMC2
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4675059copy number variation1nstd102humanUncertain significance GRCh37 chr9: 106,805,217-106,860,845 , GRCh38.p12 chr9: 104,042,936-104,098,564 SMC2, SMC2-DT
    nsv4617791copy number variation1nstd183human GRCh37 chr9: 106,856,630-106,857,039 , GRCh38.p12 chr9: 104,094,349-104,094,758 SMC2
    nsv4614694copy number variation1nstd183human GRCh37 chr9: 106,490,382-107,132,854 , GRCh38.p12 chr9: 103,728,100-104,370,573 SMC2, TOPORSLP, 6 more genes
    nsv4613449copy number variation1nstd183human GRCh37 chr9: 106,856,878-106,857,037 , GRCh38.p12 chr9: 104,094,597-104,094,756 SMC2
    nsv4610642copy number variation1nstd183human GRCh37 chr9: 106,856,702-106,857,182 , GRCh38.p12 chr9: 104,094,421-104,094,901 SMC2
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