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Items: 1 to 20 of 29

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3880914copy number variation1nstd102humanLikely benign GRCh37 chr3: 100,432,510-100,438,922 , GRCh38 chr3: 100,713,666-100,720,078 TFG
    nsv6314668copy number variation1nstd102humanLikely benign GRCh37 chr3: 100,432,520-100,438,912 , GRCh38.p12 chr3: 100,713,676-100,720,068 TFG
    nsv6314644copy number variation1nstd102humanLikely benign GRCh37 chr3: 100,432,530-100,438,922 , GRCh38.p12 chr3: 100,713,686-100,720,078 TFG
    nsv5673555copy number variation1nstd102humanLikely benign GRCh37 chr3: 100,432,530-100,438,912 , GRCh38.p12 chr3: 100,713,686-100,720,068 TFG
    nsv5673634copy number variation1nstd102humanLikely benign GRCh37 chr3: 100,432,530-100,438,902 , GRCh38.p12 chr3: 100,713,686-100,720,058 TFG
    nsv5564186copy number variation1nstd102humanUncertain significance GRCh37 chr3: 100,455,410-100,463,785 , GRCh38.p12 chr3: 100,736,566-100,744,941 TFG
    nsv6311533copy number variation1nstd102humanUncertain significance GRCh37 chr3: 100,432,530-100,467,375 , GRCh38.p12 chr3: 100,713,686-100,748,531 TFG, ABI3BP
    nsv5381356copy number variation1nstd102humanUncertain significance GRCh37 chr3: 100,463,667-100,467,385 , GRCh38.p12 chr3: 100,744,823-100,748,541 TFG, ABI3BP
    nsv3882590copy number variation1nstd102humanBenign GRCh37 chr3: 100,322,043-100,451,393 , GRCh38.p12 chr3: 100,603,199-100,732,549 TFG, ADGRG7, 1 more genes
    nsv3872217copy number variation1nstd102humanBenign GRCh37 chr3: 100,324,522-100,451,393 , GRCh38.p12 chr3: 100,605,678-100,732,549 TFG, GMFBP1, 1 more genes
    nsv3883875copy number variation1nstd102humanBenign GRCh37 chr3: 100,322,043-100,445,958 , GRCh38.p12 chr3: 100,603,199-100,727,114 TFG, ADGRG7, 1 more genes
    nsv3877586copy number variation1nstd102humanBenign GRCh37 chr3: 100,351,696-100,467,232 , GRCh38.p12 chr3: 100,632,852-100,748,388 TFG, GMFBP1, 2 more genes
    nsv3887981copy number variation1nstd102humanBenign GRCh37 chr3: 100,353,809-100,467,018 , GRCh38.p12 chr3: 100,634,965-100,748,174 TFG, GMFBP1, 2 more genes
    nsv3889624copy number variation1nstd102humanBenign GRCh37 chr3: 100,353,809-100,458,260 , GRCh38.p12 chr3: 100,634,965-100,739,416 TFG, GMFBP1, 1 more genes
    nsv3877396copy number variation1nstd102humanBenign GRCh37 chr3: 100,353,809-100,441,716 , GRCh38.p12 chr3: 100,634,965-100,722,872 TFG, GMFBP1, 1 more genes
    nsv3912540copy number variation3nstd102humanBenign/Likely benign, Benign GRCh38 chr3: 100,641,848-100,725,206 , GRCh37 chr3: 100,360,692-100,444,050 TFG, GMFBP1, 1 more genes
    nsv3886362copy number variation2nstd102humannot provided GRCh37 chr3: 100,351,696-100,437,892 , GRCh38 chr3: 100,632,852-100,719,048 TFG, GMFBP1, 1 more genes
    esv3648121copy number variation1estd216humannot provided GRCh37 chr3: 100,351,696-100,437,892 , GRCh38.p12 chr3: 100,632,852-100,719,048 TFG, ADGRG7, 1 more genes
    esv3648120copy number variation1estd216humannot provided GRCh37 chr3: 100,351,696-100,437,892 , GRCh38.p12 chr3: 100,632,852-100,719,048 TFG, ADGRG7, 1 more genes
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 TFG, NECTIN3, 418 more genes
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