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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
    nsv5945002copy number variation1nstd209human GRCh38 chr14: 67,594,589-67,595,072 , GRCh37.p13 chr14: 68,061,306-68,061,789 PIGH
    nsv5931378copy number variation1nstd209human GRCh38 chr14: 67,255,048-67,637,246 , GRCh37.p13 chr14: 67,721,765-68,103,963 , MIR5694, 11 more genes
    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
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv4838047copy number variation1nstd200human GRCh37 chr14: 67,721,720-68,104,019 , GRCh38.p12 chr14: 67,255,003-67,637,302 , PIGH, 11 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
    nsv4529257copy number variation1nstd166human GRCh37.p13 chr14: 67,433,394-68,147,101 , GRCh38.p12 chr14: 66,966,677-67,680,384 , SF3B4P1, 19 more genes
    nsv4323072inversion1nstd166human GRCh37.p13 chr14: 66,260,597-70,789,330 , GRCh38.p12 chr14: 65,793,879-70,322,613 , ACTN1, 81 more genes
    nsv4213271copy number variation1nstd166human GRCh37.p13 chr14: 68,032,197-68,278,086 , GRCh38.p12 chr14: 67,565,480-67,811,369 , PLEKHH1, 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
    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
    nsv3904265copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229 CRIP1, GPATCH2L, 1929 more genes
    nsv3903706copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 68,035,240-73,568,130 , GRCh38.p12 chr14: 67,568,523-73,101,422 ACTN1, ARG2, 108 more genes
    nsv3903256copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050 DHRS7, MIR548Y, 1946 more genes
    nsv3902883copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863 LOC440181, HEATR5A-DT, 1998 more genes
    nsv3899639copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456 LOC100289511, RNU6-552P, 1996 more genes
    nsv3168616copy number variation1nstd158human GRCh38.p12 chr14: 63,156,948-86,570,963 , GRCh37 chr14: 63,623,666-87,037,307 , ACTN1, 394 more genes
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