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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6973125copy number variation1nstd229human GRCh38 chr14: 73,200,081-73,280,986 , GRCh37.p13 chr14: 73,666,789-73,747,694 PAPLN-AS1, NUMB, 3 more genes
    nsv6969613copy number variation1nstd229human GRCh38 chr14: 73,236,009-73,247,324 , GRCh37.p13 chr14: 73,702,717-73,714,032 RNU6-419P, PAPLN-AS1, 1 more genes
    nsv6965001copy number variation1nstd229human GRCh38 chr14: 72,496,701-73,300,600 , GRCh37.p13 chr14: 72,963,409-73,767,308 NUMB, PAPLN, 17 more genes
    nsv6964071copy number variation1nstd229human GRCh38 chr14: 72,826,799-73,296,481 , GRCh37.p13 chr14: 73,293,507-73,763,189 DPF3, RPL36P3, 15 more genes
    nsv6637337copy number variation1nstd102humanUncertain significance GRCh37 chr14: 73,216,923-73,758,752 , GRCh38.p12 chr14: 72,750,215-73,292,044 NUMB, TRC-GCA8-1, 15 more genes
    nsv6477365copy number variation1nstd223human GRCh38 chr14: 72,712,342-73,303,422 , GRCh37.p13 chr14: 73,179,050-73,770,130 PAPLN-AS1, RBM25-AS1, 15 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
    nsv6132936copy number variation1nstd213human GRCh37 chr14: 73,480,000-74,470,001 , GRCh38.p12 chr14: 73,013,292-74,003,298 PSEN1, ACOT2, 32 more genes
    nsv6102931inversion1nstd212human GRCh38 chr14: 73,018,779-73,326,339 , GRCh37.p13 chr14: 73,485,487-73,793,047 PSEN1, NUMB, 8 more genes
    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
    nsv4999991copy number variation1nstd200human GRCh38 chr14: 73,239,408-73,243,001 , GRCh37.p13 chr14: 73,706,116-73,709,709 PAPLN, PAPLN-AS1
    nsv4835883copy number variation1nstd200human GRCh37 chr14: 73,706,116-73,709,709 , GRCh38.p12 chr14: 73,239,408-73,243,001 PAPLN-AS1, PAPLN
    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
    nsv3922378copy number variation1nstd102humanUncertain significance NCBI36 chr14: 72,324,025-72,805,442 , GRCh37.p13 chr14: 73,254,272-73,735,689 , GRCh38.p12 chr14: 72,787,564-73,268,981 PAPLN, RN7SL586P, 14 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
    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
    nsv3913507copy number variation1nstd102humanUncertain significance NCBI36 chr14: 72,423,225-72,903,687 , GRCh38 chr14: 72,886,764-73,367,226 , GRCh37 chr14: 73,353,472-73,833,934 RBM25-AS1, RPS12P1, 15 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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