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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116370mobile element insertion1nstd186human GRCh37 chr15: 38,769,445-38,769,496 , GRCh38.p12 chr15: 38,477,244-38,477,295 FAM98B
    nsv5972315insertion1nstd209human GRCh38 chr15: 38,475,065-38,475,065 , GRCh37.p13 chr15: 38,767,266-38,767,266 FAM98B
    nsv5970860insertion1nstd209human GRCh38 chr15: 38,477,227-38,477,227 , GRCh37.p13 chr15: 38,769,428-38,769,428 FAM98B
    nsv5939106copy number variation1nstd209human GRCh38 chr15: 38,008,106-40,186,655 , GRCh37.p13 chr15: 38,300,307-40,478,856 , LOC105370784, 36 more genes
    nsv5714295mobile element insertion2nstd211human GRCh38 chr15: 38,475,082-38,475,082 , GRCh37.p13 chr15: 38,767,283-38,767,283 FAM98B
    nsv5696223mobile element insertion2nstd211human GRCh38 chr15: 38,477,244-38,477,244 , GRCh37.p13 chr15: 38,769,445-38,769,445 FAM98B
    nsv5648216insertion1nstd207human GRCh38 chr15: 38,477,227-38,477,227 , GRCh37.p13 chr15: 38,769,428-38,769,428 FAM98B
    nsv5426052mobile element insertion1nstd206human GRCh38 chr15: 38,475,082-38,475,133 , GRCh37.p13 chr15: 38,767,283-38,767,334 FAM98B
    nsv5420950mobile element insertion1nstd206human GRCh38 chr15: 38,477,244-38,477,295 , GRCh37.p13 chr15: 38,769,445-38,769,496 FAM98B
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5159145mobile element insertion1nstd203human GRCh38 chr15: 38,477,226-38,477,244 , GRCh37.p13 chr15: 38,769,427-38,769,445 FAM98B
    nsv5156775mobile element insertion1nstd203human GRCh38 chr15: 38,477,233-38,477,244 , GRCh37.p13 chr15: 38,769,434-38,769,445 FAM98B
    nsv5156484mobile element insertion1nstd203human GRCh38 chr15: 38,485,750-38,485,766 , GRCh37.p13 chr15: 38,777,951-38,777,967 FAM98B
    nsv5153489mobile element insertion1nstd203human GRCh38 chr15: 38,455,619-38,455,632 , GRCh37.p13 chr15: 38,747,820-38,747,833 FAM98B
    nsv5150803mobile element insertion1nstd203human GRCh38 chr15: 38,477,227-38,477,242 , GRCh37.p13 chr15: 38,769,428-38,769,443 FAM98B
    nsv5149698mobile element insertion1nstd203human GRCh38 chr15: 38,477,234-38,477,244 , GRCh37.p13 chr15: 38,769,435-38,769,445 FAM98B
    nsv5149154mobile element insertion1nstd203human GRCh38 chr15: 38,475,073-38,475,082 , GRCh37.p13 chr15: 38,767,274-38,767,283 FAM98B
    nsv5144842mobile element insertion1nstd203human GRCh38 chr15: 38,475,066-38,475,082 , GRCh37.p13 chr15: 38,767,267-38,767,283 FAM98B
    nsv5143734mobile element insertion1nstd203human GRCh38 chr15: 38,477,224-38,477,241 , GRCh37.p13 chr15: 38,769,425-38,769,442 FAM98B
    nsv5142896mobile element insertion1nstd203human GRCh38 chr15: 38,477,232-38,477,244 , GRCh37.p13 chr15: 38,769,433-38,769,445 FAM98B
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