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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5489458copy number variation1nstd206human GRCh38 chr10: 52,467,970-52,469,492 , GRCh37.p13 chr10: 54,227,730-54,229,252 LNCAROD
    nsv5480060copy number variation1nstd206human GRCh38 chr10: 52,444,849-52,482,276 , GRCh37.p13 chr10: 54,204,609-54,242,036 LNCAROD
    nsv5380868copy number variation1nstd102humanUncertain significance GRCh37 chr10: 54,011,320-54,530,789 , GRCh38.p12 chr10: 52,251,560-52,771,029 RPL31P44, DKK1, 6 more genes
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4973636copy number variation1nstd200human GRCh38 chr10: 51,844,996-52,464,544 , GRCh37.p13 chr10: 53,604,756-54,224,304 RPL31P44, LNCAROD, 4 more genes
    nsv4969998copy number variation1nstd200human GRCh38 chr10: 52,456,778-52,459,922 , GRCh37.p13 chr10: 54,216,538-54,219,682 LNCAROD
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4848529copy number variation1nstd200human GRCh37 chr10: 53,604,756-54,224,304 , GRCh38.p12 chr10: 51,844,996-52,464,544 DKK1, THAP12P3, 4 more genes
    nsv4675455copy number variation1nstd102humanPathogenic GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325 MRLN, LOC102724778, 242 more genes
    nsv4675213copy number variation1nstd102humanUncertain significance GRCh37 chr10: 53,802,602-55,217,542 , GRCh38.p12 chr10: 52,042,842-53,457,782 DKK1, RPL31P44, 13 more genes
    nsv4492138mobile element insertion1nstd166human GRCh37.p13 chr10: 54,228,155-54,228,155 , GRCh38.p12 chr10: 52,468,395-52,468,395 LNCAROD
    nsv4457288copy number variation1nstd102humanUncertain significance GRCh37 chr10: 53,815,624-54,483,403 , GRCh38.p12 chr10: 52,055,864-52,723,643 PRKG1-AS1, DKK1, 5 more genes
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4313384inversion1nstd166human GRCh37.p13 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , RET, 306 more genes
    nsv4191922copy number variation1nstd166human GRCh37.p13 chr10: 54,221,373-54,221,586 , GRCh38.p12 chr10: 52,461,613-52,461,826 LNCAROD
    nsv4188408copy number variation1nstd166human GRCh37.p13 chr10: 54,074,325-54,473,137 , GRCh38.p12 chr10: 52,314,565-52,713,377 DKK1, THAP12P3, 4 more genes
    nsv4178867copy number variation1nstd166human GRCh37.p13 chr10: 53,970,817-56,409,978 , GRCh38.p12 chr10: 52,211,057-54,650,218 LOC105378307, NEFMP1, 18 more genes
    nsv4175695copy number variation1nstd166human GRCh37.p13 chr10: 54,212,813-54,216,375 , GRCh38.p12 chr10: 52,453,053-52,456,615 LNCAROD
    nsv3972371copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 49,390,457-60,061,643 , GRCh38.p12 chr10: 45,931,517-58,301,883 CHAT, CTSLP2, 156 more genes
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