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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957516insertion1nstd209human GRCh38 chr3: 154,310,807-154,310,807 , GRCh37.p13 chr3: 154,028,596-154,028,596 DHX36
    nsv5896853copy number variation1nstd209human GRCh38 chr3: 154,288,183-154,288,744 , GRCh37.p13 chr3: 154,005,972-154,006,533 DHX36
    nsv5692442mobile element insertion1nstd211human GRCh38 chr3: 154,312,887-154,312,887 , GRCh37.p13 chr3: 154,030,676-154,030,676 DHX36
    nsv5691576mobile element insertion2nstd211human GRCh38 chr3: 154,320,352-154,320,352 , GRCh37.p13 chr3: 154,038,141-154,038,141 DHX36
    nsv5439592copy number variation1nstd206human GRCh38 chr3: 154,288,193-154,288,745 , GRCh37.p13 chr3: 154,005,982-154,006,534 DHX36
    nsv5406377mobile element insertion1nstd206human GRCh38 chr3: 154,320,352-154,320,403 , GRCh37.p13 chr3: 154,038,141-154,038,192 DHX36
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5335471translocation1nstd200human GRCh37 chr3: 154,030,356-154,030,356 , GRCh37 chr3: 154,030,694-154,030,694 , GRCh38.p12 chr3: 154,312,905-154,312,905 , GRCh38.p12 chr3: 154,312,567-154,312,567 DHX36
    nsv5315153copy number variation1nstd204human GRCh38.p13 chr3: 154,306,447-154,306,733 , GRCh37.p13 chr3: 154,024,236-154,024,522 DHX36
    nsv5305457copy number variation1nstd204human GRCh38.p13 chr3: 154,312,541-154,312,927 , GRCh37.p13 chr3: 154,030,330-154,030,716 DHX36
    nsv5229845copy number variation1nstd204human GRCh38.p13 chr3: 154,286,093-154,288,219 , GRCh37.p13 chr3: 154,003,882-154,006,008 DHX36
    nsv5090972mobile element insertion1nstd203human GRCh38 chr3: 154,303,287-154,303,298 , GRCh37.p13 chr3: 154,021,076-154,021,087 DHX36
    nsv5086490mobile element insertion1nstd203human GRCh38 chr3: 154,320,338-154,320,352 , GRCh37.p13 chr3: 154,038,127-154,038,141 DHX36
    nsv5086295mobile element insertion1nstd203human GRCh38 chr3: 154,273,781-154,273,789 , GRCh37.p13 chr3: 153,991,570-153,991,578 DHX36
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4914902copy number variation1nstd200human GRCh38 chr3: 154,296,312-154,297,789 , GRCh37.p13 chr3: 154,014,101-154,015,578 DHX36
    nsv4912485copy number variation1nstd200human GRCh38 chr3: 154,291,334-154,294,268 , GRCh37.p13 chr3: 154,009,123-154,012,057 DHX36
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4469548mobile element insertion1nstd166human GRCh37.p13 chr3: 154,038,127-154,038,127 , GRCh38.p12 chr3: 154,320,338-154,320,338 DHX36
    nsv4469183mobile element insertion1nstd166human GRCh37.p13 chr3: 153,991,564-153,991,564 , GRCh38.p12 chr3: 154,273,775-154,273,775 , GRCh38.p12 chr3|NT_187533.1: 8,268-8,268 DHX36
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