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Items: 1 to 20 of 241

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145702copy number variation1nstd232human GRCh37.p13 chr3: 47,891,042-47,891,116 , GRCh38.p12 chr3: 47,849,552-47,849,626 MAP4, DHX30, 1 more genes
    nsv7143697copy number variation1nstd232human GRCh37.p13 chr3: 47,890,039-47,890,111 , GRCh38.p12 chr3: 47,848,549-47,848,621 DHX30, MIR1226
    nsv7142726copy number variation1nstd232human GRCh37.p13 chr3: 47,890,305-47,890,406 , GRCh38.p12 chr3: 47,848,815-47,848,916 MAP4, DHX30, 1 more genes
    nsv7096956copy number variation1nstd102humanUncertain significance GRCh37 chr3: 47,422,587-47,919,033 , GRCh38.p12 chr3: 47,381,097-47,877,543 BOLA2P2, RN7SL870P, 12 more genes
    nsv7096805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318 SNORA94, LIMD1-AS1, 120 more genes
    nsv7052416inversion1nstd229human GRCh38 chr3: 47,535,316-47,827,121 , GRCh37.p13 chr3: 47,576,806-47,868,611 SMARCC1, SNORD146, 5 more genes
    nsv7047381inversion1nstd229human GRCh38 chr3: 47,589,597-48,210,528 , GRCh37.p13 chr3: 47,631,087-48,252,018 CDC25A, SNORD146, 12 more genes
    nsv6717793copy number variation1nstd229human GRCh38 chr3: 47,664,822-47,841,315 , GRCh37.p13 chr3: 47,706,312-47,882,805 SMARCC1, DHX30
    nsv6710809copy number variation1nstd229human GRCh38 chr3: 47,636,001-47,953,700 , GRCh37.p13 chr3: 47,677,491-47,995,190 MAP4, SNORD146, 4 more genes
    nsv6709701copy number variation1nstd229human GRCh38 chr3: 47,793,854-47,802,225 , GRCh37.p13 chr3: 47,835,344-47,843,715 DHX30
    nsv6709380copy number variation1nstd229human GRCh38 chr3: 47,729,831-48,514,976 , GRCh37.p13 chr3: 47,771,321-48,552,409 ATRIP-TREX1, PLXNB1, 26 more genes
    nsv6706759copy number variation1nstd229human GRCh38 chr3: 47,123,901-47,954,200 , GRCh37.p13 chr3: 47,165,391-47,995,690 KIF9-AS1, LOC105377073, 18 more genes
    nsv6704186copy number variation1nstd229human GRCh38 chr3: 47,803,801-47,806,800 , GRCh37.p13 chr3: 47,845,291-47,848,290 DHX30
    nsv6703518copy number variation1nstd229human GRCh38 chr3: 47,817,019-47,817,275 , GRCh37.p13 chr3: 47,858,509-47,858,765 DHX30
    nsv6701154copy number variation1nstd229human GRCh38 chr3: 47,826,467-47,828,235 , GRCh37.p13 chr3: 47,867,957-47,869,725 DHX30
    nsv6700123copy number variation1nstd229human GRCh38 chr3: 47,827,101-48,006,500 , GRCh37.p13 chr3: 47,868,591-48,047,990 MAP4, MIR1226, 2 more genes
    nsv6628987copy number variation1nstd224human GRCh37 chr3: 47,702,865-47,882,649 , GRCh38.p12 chr3: 47,661,375-47,841,159 SMARCC1, HIGD2AP2, 2 more genes
    nsv6543325inversion1nstd223human GRCh38 chr3: 47,812,387-47,812,779 , GRCh37.p13 chr3: 47,853,877-47,854,269 DHX30
    nsv6368887copy number variation1nstd223human GRCh38 chr3: 47,830,105-47,838,243 , GRCh37.p13 chr3: 47,871,595-47,879,733 DHX30
    nsv6365976copy number variation1nstd223human GRCh38 chr3: 47,762,912-47,822,983 , GRCh37.p13 chr3: 47,804,402-47,864,473 SMARCC1, DHX30
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