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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077556inversion1nstd229human GRCh38 chr14: 73,471,057-73,821,037 , GRCh37.p13 chr14: 73,937,762-74,287,740 PNMA1, MIDEAS-AS1, 15 more genes
    nsv7074319inversion1nstd229human GRCh38 chr14: 73,491,478-73,498,101 , GRCh37.p13 chr14: 73,958,182-73,964,805 ACOT1, HEATR4, 1 more genes
    nsv7070231inversion1nstd229human GRCh38 chr14: 73,444,203-73,498,108 , GRCh37.p13 chr14: 73,910,911-73,964,812 RIOX1, ACOT1, 3 more genes
    nsv6963633copy number variation1nstd229human GRCh38 chr14: 73,486,297-73,490,763 , GRCh37.p13 chr14: 73,953,002-73,957,468 RIOX1, HEATR4
    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
    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
    nsv5939564copy number variation1nstd209human GRCh38 chr14: 73,487,523-73,496,084 , GRCh37.p13 chr14: 73,954,228-73,962,788 HEATR4, RIOX1, 1 more genes
    nsv5859567copy number variation1nstd209human GRCh38 chr14: 73,487,581-73,495,263 , GRCh37.p13 chr14: 73,954,286-73,961,967 RIOX1, ACOT1, 1 more genes
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv3961381copy number variation1nstd168human GRCh38 chr14: 73,452,756-73,592,245 , GRCh37.p13 chr14: 73,919,463-74,058,949 ACOT2, NT5CP2, 8 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
    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
    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
    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
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