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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094446copy number variation1nstd102humanUncertain significance GRCh37 chr14: 68,145,038-68,238,947 , GRCh38.p12 chr14: 67,678,321-67,772,230 RN7SL213P, RPL21P9, 4 more genes
    nsv7078008inversion1nstd229human GRCh38 chr14: 60,214,891-67,756,686 , GRCh37.p13 chr14: 60,681,609-68,223,403 ATP6V1D, LOC101927756, 129 more genes
    nsv7077538inversion1nstd229human GRCh38 chr14: 63,703,374-67,849,523 , GRCh37.p13 chr14: 64,170,092-68,316,240 RPPH1-2P, SYNE2, 75 more genes
    nsv7068193inversion1nstd229human GRCh38 chr14: 65,793,880-70,322,609 , GRCh37.p13 chr14: 66,260,598-70,789,326 BANF1P1, GALNT16-AS1, 78 more genes
    nsv7058984inversion1nstd229human GRCh38 chr14: 65,563,947-68,493,504 , GRCh37.p13 chr14: 66,030,665-68,960,221 RN7SL108P, GPHN, 40 more genes
    nsv6974298copy number variation1nstd229human GRCh38 chr14: 67,696,208-67,696,373 , GRCh37.p13 chr14: 68,162,925-68,163,090 RDH11
    nsv6969504copy number variation1nstd229human GRCh38 chr14: 67,690,034-67,690,363 , GRCh37.p13 chr14: 68,156,751-68,157,080 RDH11
    nsv6969160copy number variation1nstd229human GRCh38 chr14: 67,653,401-67,677,400 , GRCh37.p13 chr14: 68,120,118-68,144,117 VTI1B, RDH11, 1 more genes
    nsv6967690copy number variation1nstd229human GRCh38 chr14: 67,565,480-67,811,369 , GRCh37.p13 chr14: 68,032,197-68,278,086 HMGB1P34, LOC100419668, 13 more genes
    nsv6966754copy number variation1nstd229human GRCh38 chr14: 67,682,001-67,684,600 , GRCh37.p13 chr14: 68,148,718-68,151,317 RDH11
    nsv6591861inversion1nstd223human GRCh38 chr14: 65,793,878-70,322,614 , GRCh37.p13 chr14: 66,260,596-70,789,331 SLC8A3, GALNT16-AS1, 78 more genes
    nsv6476063copy number variation1nstd223human GRCh38 chr14: 64,354,345-74,200,229 , GRCh37.p13 chr14: 64,821,063-74,666,932 RNU6-240P, COX7A2P1, 196 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
    nsv6314209copy number variation1nstd102humanUncertain significance GRCh37 chr14: 67,443,801-68,153,682 , GRCh38.p12 chr14: 66,977,084-67,686,965 PLEK2, EIF2S1, 18 more genes
    nsv6309557copy number variation1nstd102humanUncertain significance GRCh37 chr14: 68,145,038-68,282,680 , GRCh38.p12 chr14: 67,678,321-67,815,963 RN7SL213P, RPL21P9, 5 more genes
    nsv6132933copy number variation1nstd213human GRCh37 chr14: 68,060,000-68,660,001 , GRCh38.p12 chr14: 67,593,283-68,193,284 ARG2, VTI1B, 16 more genes
    nsv6034858copy number variation1nstd212human GRCh38 chr14: 67,686,522-67,686,585 , GRCh37.p13 chr14: 68,153,239-68,153,302 RDH11
    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
    nsv5539577insertion1nstd206human GRCh38 chr14: 67,694,448-67,694,487 , GRCh37.p13 chr14: 68,161,165-68,161,204 RDH11
    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
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