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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6976835copy number variation1nstd229human GRCh38 chr14: 75,266,749-75,309,978 , GRCh37.p13 chr14: 75,733,452-75,776,681 LINC01220, DPPA5P4, 1 more genes
    nsv6971631copy number variation1nstd229human GRCh38 chr14: 75,233,901-75,313,900 , GRCh37.p13 chr14: 75,700,604-75,780,603 LINC01220, DPPA5P4, 1 more genes
    nsv6967574copy number variation1nstd229human GRCh38 chr14: 75,169,301-75,380,900 , GRCh37.p13 chr14: 75,636,004-75,847,603 DPPA5P4, TMED10, 3 more genes
    nsv6964648copy number variation1nstd229human GRCh38 chr14: 75,255,601-75,729,300 , GRCh37.p13 chr14: 75,722,304-76,195,643 LOC107984653, ERG28, 12 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6241531mobile element insertion1nstd215human GRCh38 chr14: 75,277,672-75,277,672 , GRCh37.p13 chr14: 75,744,375-75,744,375 FOS
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv4630226copy number variation1nstd183human GRCh37 chr14: 75,740,542-75,763,164 , GRCh38.p12 chr14: 75,273,839-75,296,461 FOS, DPPA5P4, 1 more genes
    nsv4372472copy number variation1nstd173human GRCh37 chr14: 75,643,603-75,755,680 , GRCh38.p12 chr14: 75,176,900-75,288,977 TMED10, RNU4ATAC14P, 1 more genes
    nsv4349747copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 74,040,231-76,368,547 , GRCh38.p12 chr14: 73,573,527-75,902,204 ACYP1, ENTPD5, 72 more genes
    nsv4220896copy number variation1nstd166human GRCh37.p13 chr14: 75,738,000-75,747,000 , GRCh38.p12 chr14: 75,271,297-75,280,297 FOS
    nsv3924066copy number variation1nstd102humanUncertain significance GRCh37 chr14: 75,452,898-76,865,601 , GRCh38 chr14: 74,986,195-76,399,258 , NCBI36 chr14: 74,522,651-75,935,354 RPS24P2, EIF2B2, 29 more genes
    nsv3923727copy number variation1nstd102humanPathogenic GRCh37 chr14: 70,028,816-82,441,728 , GRCh38 chr14: 69,562,099-81,975,384 , NCBI36 chr14: 69,098,569-81,511,481 CEP128, COX6CP11, 240 more genes
    nsv3923448copy number variation1nstd102humanPathogenic NCBI36 chr14: 73,413,528-77,578,518 , GRCh38 chr14: 73,877,072-78,042,422 , GRCh37 chr14: 74,343,775-78,508,765 ZC2HC1C, RPL21P10, 113 more genes
    nsv3922094copy number variation1nstd102humanPathogenic GRCh38 chr14: 73,655,772-106,879,298 , GRCh37 chr14: 74,122,475-107,287,505 , NCBI36 chr14: 73,192,228-106,358,550 LOC105370614, LOC105370617, 849 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
    nsv3919051copy number variation1nstd102humanLikely pathogenic NCBI36 chr14: 72,879,674-78,371,155 , GRCh37 chr14: 73,809,921-79,301,402 , GRCh38 chr14: 73,343,213-78,835,059 ACYP1, ENTPD5, 137 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 MIR656, TRAJ59, 1918 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 BANF1P1, IGHV1-68, 1996 more genes
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