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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv4627767copy number variation1nstd183human GRCh37 chr14: 76,023,819-76,300,735 , GRCh38.p12 chr14: 75,557,476-75,834,392 , ERG28, 6 more genes
    nsv4515437mobile element insertion1nstd166human GRCh37.p13 chr14: 76,126,695-76,126,695 , GRCh38.p12 chr14: 75,660,352-75,660,352 ERG28, TTLL5
    nsv4501073mobile element insertion1nstd166human GRCh37.p13 chr14: 76,120,941-76,120,941 , GRCh38.p12 chr14: 75,654,598-75,654,598 ERG28
    nsv4456104copy number variation1nstd102humanUncertain significance GRCh37 chr14: 76,057,971-76,576,494 , GRCh38.p12 chr14: 75,591,628-76,110,151 RPS24P2, TGFB3, 8 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
    nsv4228539copy number variation1nstd166human GRCh37.p13 chr14: 76,122,157-76,122,253 , GRCh38.p12 chr14: 75,655,814-75,655,910 ERG28
    nsv4218030copy number variation1nstd166human GRCh37.p13 chr14: 76,118,156-76,118,465 , GRCh38.p12 chr14: 75,651,813-75,652,122 ERG28
    nsv4212664copy number variation1nstd166human GRCh37.p13 chr14: 76,127,672-76,127,856 , GRCh38.p12 chr14: 75,661,329-75,661,513 TTLL5, ERG28
    nsv3955687copy number variation1nstd168human GRCh38 chr14: 75,624,632-75,652,025 , GRCh37.p13 chr14: 76,090,975-76,118,368 ERG28, FLVCR2
    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
    nsv3922441copy number variation1nstd102humanPathogenic GRCh38 chr14: 75,489,052-79,610,332 , GRCh37 chr14: 75,955,395-80,076,675 , NCBI36 chr14: 75,025,148-79,146,428 IRF2BPL, LOC105370583, 69 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
    nsv3921475copy number variation1nstd102humanUncertain significance NCBI36 chr14: 75,025,148-75,504,061 , GRCh37 chr14: 75,955,395-76,434,308 , GRCh38 chr14: 75,489,052-75,967,965 TGFB3, RPS24P2, 9 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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