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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5672576copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 68,195,898-68,200,575 , GRCh38.p12 chr14: 67,729,181-67,733,858 ZFYVE26, RDH12
    nsv5506165copy number variation1nstd206human GRCh38 chr14: 67,732,127-67,740,893 , GRCh37.p13 chr14: 68,198,844-68,207,610 RDH12, ZFYVE26
    nsv5505723copy number variation1nstd206human GRCh38 chr14: 67,711,036-67,718,244 , GRCh37.p13 chr14: 68,177,753-68,184,961 RPL21P9, RDH12
    nsv5380972copy number variation2nstd102humanUncertain significance GRCh37 chr14: 65,937,790-68,354,021 , GRCh38.p12 chr14: 65,471,072-67,887,304 RPL21P9, LOC100419668, 35 more genes
    nsv5198237mobile element insertion1nstd203human GRCh38 chr14: 67,705,467-67,705,476 , GRCh37.p13 chr14: 68,172,184-68,172,193 RN7SL369P, RDH12
    nsv5149288mobile element insertion1nstd203human GRCh38 chr14: 67,702,292-67,702,308 , GRCh37.p13 chr14: 68,169,009-68,169,025 RDH12
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5004728copy number variation1nstd200human GRCh38 chr14: 67,732,312-67,878,162 , GRCh37.p13 chr14: 68,199,029-68,344,879 RN7SL213P, RAD51B, 3 more genes
    nsv4675709copy number variation1nstd102humanUncertain significance GRCh37 chr14: 67,331,167-68,451,970 , GRCh38.p12 chr14: 66,864,449-67,985,253 RDH11, RN7SL369P, 25 more genes
    nsv4675260copy number variation1nstd102humanUncertain significance GRCh37 chr14: 68,037,409-68,278,365 , GRCh38.p12 chr14: 67,570,692-67,811,648 PLEKHH1, RDH11, 13 more genes
    nsv4627435copy number variation1nstd183human GRCh37 chr14: 68,140,879-68,191,122 , GRCh38.p12 chr14: 67,674,162-67,724,405 RDH12, RN7SL369P, 3 more genes
    nsv4619249copy number variation1nstd183human GRCh37 chr14: 68,177,733-68,184,942 , GRCh38.p12 chr14: 67,711,016-67,718,225 RDH12, RPL21P9
    nsv4509545mobile element insertion1nstd166human GRCh37.p13 chr14: 68,174,363-68,174,363 , GRCh38.p12 chr14: 67,707,646-67,707,646 RDH12
    nsv4457296copy number variation1nstd102humanUncertain significance GRCh37 chr14: 68,148,448-69,073,242 , GRCh38.p12 chr14: 67,681,731-68,606,525 LOC107984016, PPIAP6, 14 more genes
    nsv4456152copy number variation1nstd102humanUncertain significance GRCh37 chr14: 68,149,933-68,176,159 , GRCh38.p12 chr14: 67,683,216-67,709,442 RN7SL369P, RDH12, 1 more genes
    nsv4455214copy number variation1nstd102humanUncertain significance GRCh37 chr14: 68,130,744-68,275,342 , GRCh38.p12 chr14: 67,664,027-67,808,625 RN7SL213P, RPL21P9, 6 more genes
    nsv4436741copy number variation1nstd102humanUncertain significance GRCh37 chr14: 68,110,557-68,283,783 , GRCh38.p12 chr14: 67,643,840-67,817,066 RN7SL213P, RNA5SP386, 9 more genes
    nsv4426545copy number variation1nstd174human GRCh37 chr14: 68,169,401-68,181,608 , GRCh38.p12 chr14: 67,702,684-67,714,891 RPL21P9, RN7SL369P, 1 more genes
    nsv4425683copy number variation1nstd174human GRCh37 chr14: 68,177,399-68,185,067 , GRCh38.p12 chr14: 67,710,682-67,718,350 RDH12, RPL21P9
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