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Items: 1 to 20 of 399

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124715insertion1nstd186human GRCh37 chrX: 118,781,932-118,781,983 , GRCh38.p12 chrX: 119,647,969-119,648,020 SEPTIN6
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5950014insertion1nstd209human GRCh38 chrX: 119,647,970-119,647,970 , GRCh37.p13 chrX: 118,781,933-118,781,933 SEPTIN6
    nsv5887334copy number variation1nstd209human GRCh38 chrX: 119,471,365-121,073,821 , GRCh37.p13 chrX: 118,605,328-120,207,675 , LOC105373328, 56 more genes
    nsv5876936copy number variation1nstd209human GRCh38 chrX: 119,645,166-119,645,787 , GRCh37.p13 chrX: 118,779,129-118,779,750 MIR766, SEPTIN6
    nsv5726707mobile element insertion1nstd211human GRCh38 chrX: 119,678,634-119,678,634 , GRCh37.p13 chrX: 118,812,597-118,812,597 SEPTIN6
    nsv5617338insertion1nstd207human GRCh38 chrX: 119,647,958-119,647,958 , GRCh37.p13 chrX: 118,781,921-118,781,921 SEPTIN6
    nsv5548822insertion1nstd206human GRCh38 chrX: 119,647,969-119,648,020 , GRCh37.p13 chrX: 118,781,932-118,781,983 SEPTIN6
    nsv5429376copy number variation1nstd206human GRCh38 chrX: 119,678,262-119,679,627 , GRCh37.p13 chrX: 118,812,225-118,813,590 SEPTIN6
    nsv5347256translocation1nstd200human GRCh38 chr7: 81,419,138-81,419,138 , GRCh38 chrX: 119,645,675-119,645,675 , GRCh37.p13 chrX: 118,779,638-118,779,638 , GRCh37.p13 chr7: 81,048,454-81,048,454 MIR766, SEPTIN6
    nsv5338424translocation1nstd200human GRCh37 chr7: 81,048,454-81,048,454 , GRCh37 chrX: 118,779,638-118,779,638 , GRCh38.p12 chrX: 119,645,675-119,645,675 , GRCh38.p12 chr7: 81,419,138-81,419,138 MIR766, SEPTIN6
    nsv5197728mobile element insertion1nstd203human GRCh38 chrX: 119,647,929-119,647,969 , GRCh37.p13 chrX: 118,781,892-118,781,932 SEPTIN6
    nsv5197549mobile element insertion1nstd203human GRCh38 chrX: 119,647,928-119,647,969 , GRCh37.p13 chrX: 118,781,891-118,781,932 SEPTIN6
    nsv5196330mobile element insertion1nstd203human GRCh38 chrX: 119,647,963-119,647,969 , GRCh37.p13 chrX: 118,781,926-118,781,932 SEPTIN6
    nsv5195035mobile element insertion1nstd203human GRCh38 chrX: 119,647,960-119,647,969 , GRCh37.p13 chrX: 118,781,923-118,781,932 SEPTIN6
    nsv5193107mobile element insertion1nstd203human GRCh38 chrX: 119,647,925-119,647,969 , GRCh37.p13 chrX: 118,781,888-118,781,932 SEPTIN6
    nsv5192819mobile element insertion1nstd203human GRCh38 chrX: 119,647,912-119,647,969 , GRCh37.p13 chrX: 118,781,875-118,781,932 SEPTIN6
    nsv5192020mobile element insertion1nstd203human GRCh38 chrX: 119,647,939-119,647,969 , GRCh37.p13 chrX: 118,781,902-118,781,932 SEPTIN6
    nsv5191906mobile element insertion1nstd203human GRCh38 chrX: 119,647,936-119,647,969 , GRCh37.p13 chrX: 118,781,899-118,781,932 SEPTIN6
    nsv5191355mobile element insertion1nstd203human GRCh38 chrX: 119,647,959-119,647,969 , GRCh37.p13 chrX: 118,781,922-118,781,932 SEPTIN6
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