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Items: 1 to 20 of 58

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093048copy number variation1nstd102humanLikely benign GRCh37 chr19: 55,667,866-55,667,964 , GRCh38 chr19: 55,156,498-55,156,596 TNNI3
    nsv3873375copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,663,182-55,666,218 , GRCh38 chr19: 55,151,814-55,154,850 TNNI3
    nsv6310650copy number variation2nstd102humanUncertain significance GRCh37 chr19: 55,663,202-55,666,218 , GRCh38.p12 chr19: 55,151,834-55,154,850 TNNI3
    nsv4682249copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,663,192-55,666,208 , GRCh38.p12 chr19: 55,151,824-55,154,840 TNNI3
    nsv4682133copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,665,388-55,668,022 , GRCh38.p12 chr19: 55,154,020-55,156,654 TNNI3
    nsv7095671copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,663,207-55,664,624 , GRCh38.p12 chr19: 55,151,839-55,153,256 TNNI3
    nsv7096959copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,485,283-52,485,425 , GRCh38.p12 chr3: 52,451,267-52,451,409 TNNC1
    nsv4349152copy number variation1nstd102humanPathogenic GRCh37 chr19: 55,652,193-55,665,240 , GRCh38.p12 chr19: 55,140,825-55,153,872 TNNI3, TNNT1
    nsv4451628copy number variation1nstd102humanPathogenic GRCh37 chr19: 55,652,231-55,663,305 , GRCh38 chr19: 55,140,863-55,151,937 TNNI3, TNNT1
    nsv4682620copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,652,241-55,663,295 , GRCh38.p12 chr19: 55,140,873-55,151,927 TNNI3, TNNT1
    nsv7095224copy number variation1nstd102humanPathogenic GRCh37 chr19: 55,644,283-55,678,016 , GRCh38.p12 chr19: 55,132,915-55,166,648 TNNT1, DNAAF3, 2 more genes
    nsv6310553copy number variation2nstd102humanUncertain significance GRCh37 chr19: 55,667,549-55,668,957 , GRCh38.p12 chr19: 55,156,181-55,157,589 DNAAF3, TNNI3, 1 more genes
    nsv3909319copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,665,527-55,692,769 , GRCh38.p12 chr19: 55,154,159-55,181,401 TNNI3, DNAAF3-AS1, 3 more genes
    nsv7095670copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,644,283-55,668,957 , GRCh38.p12 chr19: 55,132,915-55,157,589 DNAAF3, TNNI3, 2 more genes
    nsv6310707copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,663,202-55,678,016 , GRCh38.p12 chr19: 55,151,834-55,166,648 DNAAF3, TNNI3, 1 more genes
    nsv4681942copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,663,192-55,669,009 , GRCh38.p12 chr19: 55,151,824-55,157,641 DNAAF3, TNNI3, 1 more genes
    nsv3882967copy number variation1nstd102humanUncertain significance GRCh38 chr19: 55,151,814-55,157,609 , GRCh37.p13 chr19: 55,663,182-55,668,977 DNAAF3-AS1, TNNI3, 1 more genes
    nsv7095225copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,663,202-55,668,957 , GRCh38.p12 chr19: 55,151,834-55,157,589 TNNI3, DNAAF3-AS1, 1 more genes
    nsv3875047copy number variation1nstd102humanPathogenic GRCh37 chr3: 52,086,599-59,689,209 , GRCh38.p12 chr3: 52,052,583-59,703,483 TNNC1, SLMAP, 132 more genes
    nsv3912778copy number variation1nstd102humanPathogenic GRCh37 chr3: 49,498,433-55,348,528 , GRCh38 chr3: 49,461,000-55,314,500 , NCBI36 chr3: 49,473,437-55,323,568 TNNC1, SEMA3G, 160 more genes
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