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Items: 1 to 20 of 80

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5319080copy number variation1nstd204human GRCh37.p13 chr10: 53,189,906-54,198,554 , GRCh38.p13 chr10: 51,430,146-52,438,794 PRKG1, DKK1, 4 more genes
    nsv5254463copy number variation1nstd204human GRCh38.p13 chr10: 52,258,401-52,438,800 , GRCh37.p13 chr10: 54,018,161-54,198,560 DKK1, THAP12P3, 3 more genes
    nsv5246617copy number variation1nstd204human GRCh38.p13 chr10: 52,300,098-52,334,773 , GRCh37.p13 chr10: 54,059,858-54,094,533 PRKG1-AS1, DKK1
    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
    nsv4973630copy number variation1nstd200human GRCh38 chr10: 51,537,991-52,321,754 , GRCh37.p13 chr10: 53,297,751-54,081,514 CSTF2T, PRKG1, 2 more genes
    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
    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
    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
    nsv4180158copy number variation1nstd166human GRCh37.p13 chr10: 54,070,345-54,089,934 , GRCh38.p12 chr10: 52,310,585-52,330,174 PRKG1-AS1, DKK1
    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
    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
    nsv3924859copy number variation1nstd102humanPathogenic NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961 BMS1P4-AGAP5, MTCO2P23, 471 more genes
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