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Items: 1 to 20 of 533

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958598insertion1nstd209human GRCh38 chr9: 135,727,086-135,727,086 , GRCh37.p13 chr9: 138,618,932-138,618,932 KCNT1
    nsv5926228copy number variation1nstd209human GRCh38 chr9: 135,768,958-135,769,035 , GRCh37.p13 chr9: 138,660,804-138,660,881 KCNT1
    nsv5925886copy number variation1nstd209human GRCh38 chr9: 135,752,924-135,753,014 , GRCh37.p13 chr9: 138,644,770-138,644,860 KCNT1
    nsv5924417copy number variation1nstd209human GRCh38 chr9: 135,740,844-135,740,923 , GRCh37.p13 chr9: 138,632,690-138,632,769 KCNT1
    nsv5924267copy number variation1nstd209human GRCh38 chr9: 135,767,971-135,768,086 , GRCh37.p13 chr9: 138,659,817-138,659,932 KCNT1
    nsv5923328copy number variation1nstd209human GRCh38 chr9: 135,733,264-135,733,610 , GRCh37.p13 chr9: 138,625,110-138,625,456 KCNT1
    nsv5920968copy number variation1nstd209human GRCh38 chr9: 135,774,444-135,774,507 , GRCh37.p13 chr9: 138,666,290-138,666,353 KCNT1
    nsv5918202copy number variation1nstd209human GRCh38 chr9: 135,784,904-135,784,960 , GRCh37.p13 chr9: 138,676,750-138,676,806 KCNT1
    nsv5910173copy number variation1nstd209human GRCh38 chr9: 135,758,181-135,758,272 , GRCh37.p13 chr9: 138,650,027-138,650,118 KCNT1
    nsv5849877copy number variation1nstd209human GRCh38 chr9: 135,784,073-135,785,249 , GRCh37.p13 chr9: 138,675,919-138,677,095 , KCNT1
    nsv5674067copy number variation1nstd102humanLikely benign GRCh37 chr9: 138,606,413-138,606,576 , GRCh38.p12 chr9: 135,714,567-135,714,730 KCNT1
    nsv5642819insertion1nstd207human GRCh38 chr9: 135,758,167-135,758,167 , GRCh37.p13 chr9: 138,650,013-138,650,013 KCNT1
    nsv5642058insertion1nstd207human GRCh38 chr9: 135,707,729-135,707,729 , GRCh37.p13 chr9: 138,599,575-138,599,575 KCNT1
    nsv5640768insertion1nstd207human GRCh38 chr9: 135,733,433-135,733,433 , GRCh37.p13 chr9: 138,625,279-138,625,279 KCNT1
    nsv5640024insertion1nstd207human GRCh38 chr9: 135,789,062-135,789,062 , GRCh37.p13 chr9: 138,680,908-138,680,908 LOC107987140, KCNT1
    nsv5635810insertion1nstd207human GRCh38 chr9: 135,727,086-135,727,086 , GRCh37.p13 chr9: 138,618,932-138,618,932 KCNT1
    nsv5634766insertion1nstd207human GRCh38 chr9: 135,769,139-135,769,139 , GRCh37.p13 chr9: 138,660,985-138,660,985 KCNT1
    nsv5630121insertion1nstd207human GRCh38 chr9: 135,726,932-135,726,932 , GRCh37.p13 chr9: 138,618,778-138,618,778 KCNT1
    nsv5629478insertion1nstd207human GRCh38 chr9: 135,758,052-135,758,052 , GRCh37.p13 chr9: 138,649,898-138,649,898 KCNT1
    nsv5600654copy number variation1nstd207human GRCh38 chr9: 135,754,002-135,754,065 , GRCh37.p13 chr9: 138,645,848-138,645,911 KCNT1
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