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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5901935copy number variation1nstd209human GRCh38 chr5: 178,076,060-178,151,307 , GRCh37.p13 chr5: 177,503,061-177,578,308 N4BP3, NHP2, 2 more genes
    nsv5842224copy number variation1nstd209human GRCh38 chr5: 178,133,508-178,134,507 , GRCh37.p13 chr5: 177,560,509-177,561,508 RMND5B
    nsv5694148mobile element insertion2nstd211human GRCh38 chr5: 178,132,751-178,132,751 , GRCh37.p13 chr5: 177,559,752-177,559,752 RMND5B
    nsv5467233copy number variation1nstd206human GRCh38 chr5: 178,132,054-178,133,894 , GRCh37.p13 chr5: 177,559,055-177,560,895 RMND5B
    nsv5465523copy number variation1nstd206human GRCh38 chr5: 177,669,324-179,310,000 , GRCh37.p13 chr5: 177,096,325-178,737,001 , LOC100129457, 48 more genes
    nsv5458942copy number variation1nstd206human GRCh38 chr5: 178,144,531-178,144,609 , GRCh37.p13 chr5: 177,571,532-177,571,610 RMND5B
    nsv5082232mobile element insertion1nstd203human GRCh38 chr5: 178,133,555-178,133,563 , GRCh37.p13 chr5: 177,560,556-177,560,564 RMND5B
    nsv4949271copy number variation1nstd200human GRCh38 chr5: 178,143,124-178,143,375 , GRCh37.p13 chr5: 177,570,125-177,570,376 RMND5B
    nsv4940050copy number variation1nstd200human GRCh38 chr5: 178,132,254-178,137,133 , GRCh37.p13 chr5: 177,559,255-177,564,134 RMND5B
    nsv4940049copy number variation1nstd200human GRCh38 chr5: 178,132,028-178,133,910 , GRCh37.p13 chr5: 177,559,029-177,560,911 RMND5B
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4763538inversion1nstd199human GRCh37 chr5: 170,260,689-178,183,120 , GRCh38.p12 chr5: 170,833,685-178,756,119 , BNIP1, 194 more genes
    nsv4729145copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,383,384-177,926,234 , GRCh38.p12 chr5: 177,956,383-178,499,233 N4BP3, RN7SL646P, 17 more genes
    nsv4683279copy number variation2nstd102humanUncertain significance GRCh37 chr5: 177,576,694-177,580,838 , GRCh38.p12 chr5: 178,149,693-178,153,837 RMND5B, NHP2
    nsv4681216copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,027,192-177,580,838 , GRCh38.p12 chr5: 177,600,191-178,153,837 LOC100419951, B4GALT7, 17 more genes
    nsv4680563copy number variation1nstd189human GRCh37.p13 chr5: 177,523,135-177,968,962 , GRCh38.p12 chr5: 178,096,134-178,541,961 , HNRNPAB, 11 more genes
    nsv4590644copy number variation1nstd183human GRCh37 chr5: 177,374,435-177,841,487 , GRCh38.p12 chr5: 177,947,434-178,414,486 , PHYKPL, 18 more genes
    nsv4491549mobile element insertion1nstd166human GRCh37.p13 chr5: 177,558,952-177,558,952 , GRCh38.p12 chr5: 178,131,951-178,131,951 RMND5B
    nsv4457212copy number variation1nstd102humanUncertain significance GRCh37 chr5: 176,643,613-179,085,551 , GRCh38.p12 chr5: 177,216,612-179,658,550 LOC100502572, PIGFP1, 79 more genes
    nsv4455497copy number variation1nstd102humanPathogenic GRCh37 chr5: 176,848,982-180,719,789 , GRCh38.p12 chr5: 177,421,981-181,292,788 HEIH, MGAT4B, 149 more genes
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