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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146219copy number variation1nstd232human GRCh37.p13 chr3: 52,559,118-52,559,222 , GRCh38.p12 chr3: 52,525,102-52,525,206 NT5DC2
    nsv7144942copy number variation1nstd232human GRCh37.p13 chr3: 52,561,734-52,561,843 , GRCh38.p12 chr3: 52,527,718-52,527,827 NT5DC2
    nsv7144521copy number variation1nstd232human GRCh37.p13 chr3: 52,558,897-52,558,977 , GRCh38.p12 chr3: 52,524,881-52,524,961 STAB1, NT5DC2
    nsv7141230insertion1nstd232human GRCh37.p13 chr3: 52,563,351-52,563,351 , GRCh38.p12 chr3: 52,529,335-52,529,335 NT5DC2
    nsv7097206copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,109,903-53,164,416 , GRCh38.p12 chr3: 52,075,887-53,130,400 PHF7, SEMA3G, 47 more genes
    nsv7096813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406 DNAH1, BAP1, 62 more genes
    nsv7055197inversion1nstd229human GRCh38 chr3: 52,426,847-52,608,000 , GRCh37.p13 chr3: 52,460,863-52,642,016 STAB1, PBRM1, 7 more genes
    nsv6716819copy number variation1nstd229human GRCh38 chr3: 52,514,797-52,536,674 , GRCh37.p13 chr3: 52,548,813-52,570,690 UQCC5, STAB1, 1 more genes
    nsv6711686copy number variation1nstd229human GRCh38 chr3: 51,850,901-52,533,900 , GRCh37.p13 chr3: 51,884,917-52,567,916 LOC105377088, GLYCTK-AS1, 37 more genes
    nsv6706894copy number variation1nstd229human GRCh38 chr3: 52,524,121-52,531,005 , GRCh37.p13 chr3: 52,558,137-52,565,021 NT5DC2, STAB1
    nsv6706308copy number variation1nstd229human GRCh38 chr3: 52,528,296-52,531,122 , GRCh37.p13 chr3: 52,562,312-52,565,138 NT5DC2
    nsv6706207copy number variation1nstd229human GRCh38 chr3: 52,526,658-52,530,604 , GRCh37.p13 chr3: 52,560,674-52,564,620 NT5DC2
    nsv6704998copy number variation1nstd229human GRCh38 chr3: 52,523,756-52,523,870 , GRCh37.p13 chr3: 52,557,772-52,557,886 NT5DC2, STAB1
    nsv6700890copy number variation1nstd229human GRCh38 chr3: 52,237,701-52,533,900 , GRCh37.p13 chr3: 52,271,717-52,567,916 STAB1, TWF2, 16 more genes
    nsv6700789copy number variation1nstd229human GRCh38 chr3: 52,529,168-52,533,846 , GRCh37.p13 chr3: 52,563,184-52,567,862 NT5DC2
    nsv6369827copy number variation1nstd223human GRCh38 chr3: 52,164,358-54,467,618 , GRCh37.p13 chr3: 52,198,374-54,501,645 SEMA3G, STAB1, 61 more genes
    nsv6134815copy number variation1nstd213human GRCh37 chr3: 52,350,000-53,060,001 , GRCh38.p12 chr3: 52,315,984-53,025,985 ITIH1, ITIH3, 32 more genes
    nsv5903173copy number variation1nstd209human GRCh38 chr3: 52,532,799-52,532,864 , GRCh37.p13 chr3: 52,566,815-52,566,880 NT5DC2
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5439445copy number variation1nstd206human GRCh38 chr3: 52,533,777-52,533,896 , GRCh37.p13 chr3: 52,567,793-52,567,912 NT5DC2
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