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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5904288copy number variation1nstd209human GRCh38 chr4: 2,841,683-2,841,855 , GRCh37.p13 chr4: 2,843,410-2,843,582 ADD1
    nsv5900413copy number variation1nstd209human GRCh38 chr4: 2,870,400-2,870,493 , GRCh37.p13 chr4: 2,872,127-2,872,220 ADD1
    nsv5717010mobile element insertion1nstd211human GRCh38 chr4: 2,872,909-2,872,909 , GRCh37.p13 chr4: 2,874,636-2,874,636 ADD1
    nsv5675713mobile element insertion1nstd211human GRCh38 chr4: 2,887,432-2,887,432 , GRCh37.p13 chr4: 2,889,159-2,889,159 ADD1
    nsv5673743copy number variation1nstd102humanPathogenic GRCh37 chr4: 2,200,251-5,710,240 , GRCh38.p12 chr4: 2,198,524-5,708,513 ZFYVE28, LINC01587, 81 more genes
    nsv5578165copy number variation1nstd207human GRCh38 chr4: 2,870,400-2,870,493 , GRCh37.p13 chr4: 2,872,127-2,872,220 ADD1
    nsv5453593copy number variation1nstd206human GRCh38 chr4: 2,841,689-2,841,856 , GRCh37.p13 chr4: 2,843,416-2,843,583 ADD1
    nsv5441933copy number variation1nstd206human GRCh38 chr4: 2,863,986-2,865,928 , GRCh37.p13 chr4: 2,865,713-2,867,655 ADD1
    nsv5395118mobile element insertion1nstd206human GRCh38 chr4: 2,887,432-2,887,479 , GRCh37.p13 chr4: 2,889,159-2,889,206 ADD1
    nsv5386663copy number variation3nstd186human GRCh37 chr4: 2,843,416-2,843,583 , GRCh38.p12 chr4: 2,841,689-2,841,856 ADD1
    nsv5381775copy number variation1nstd102humanPathogenic GRCh37 chr4: 388,344-3,872,380 , GRCh38.p12 chr4: 394,555-3,870,653 RN7SL671P, HTT-AS, 96 more genes
    nsv5314111copy number variation1nstd204human GRCh38.p13 chr4: 2,841,679-2,841,865 , GRCh37.p13 chr4: 2,843,406-2,843,592 ADD1
    nsv5235636copy number variation1nstd204human GRCh38.p13 chr4: 2,809,001-2,893,100 , GRCh37.p13 chr4: 2,810,728-2,894,827 ADD1, SH3BP2
    nsv5169062mobile element insertion1nstd203human GRCh38 chr4: 2,858,891-2,858,907 , GRCh37.p13 chr4: 2,860,618-2,860,634 ADD1
    nsv5082073mobile element insertion1nstd203human GRCh38 chr4: 2,853,106-2,853,126 , GRCh37.p13 chr4: 2,854,833-2,854,853 ADD1
    nsv4912908copy number variation1nstd200human GRCh38 chr4: 2,841,689-2,841,856 , GRCh37.p13 chr4: 2,843,416-2,843,583 ADD1
    nsv4799173copy number variation1nstd200human GRCh37 chr4: 2,846,219-2,848,172 , GRCh38.p12 chr4: 2,844,492-2,846,445 ADD1
    nsv4799172copy number variation1nstd200human GRCh37 chr4: 2,843,416-2,843,583 , GRCh38.p12 chr4: 2,841,689-2,841,856 ADD1
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