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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4991404copy number variation1nstd200human GRCh38 chr14: 101,057,673-101,057,863 , GRCh37.p13 chr14: 101,524,010-101,524,200 MIR154
    nsv4219178copy number variation1nstd166human GRCh37.p13 chr14: 101,524,010-101,524,200 , GRCh38.p12 chr14: 101,057,673-101,057,863 MIR154
    esv2106147copy number variation1estd194human NCBI36 chr14: 100,594,796-100,594,797 , GRCh37.p13 chr14: 101,525,043-101,525,044 , GRCh38.p12 chr14: 101,058,706-101,058,707 MIR496, MIR154
    nsv1762385short tandem repeat2nstd128human GRCh37 chr14: 101,525,043-101,525,053 , GRCh38.p12 chr14: 101,058,706-101,058,716 MIR154, MIR496
    nsv6959523copy number variation1nstd229human GRCh38 chr14: 101,059,889-101,063,376 , GRCh37.p13 chr14: 101,526,226-101,529,713 MIR409, MIR496, 3 more genes
    nsv6977980copy number variation1nstd229human GRCh38 chr14: 101,058,901-101,061,200 , GRCh37.p13 chr14: 101,525,238-101,527,537 MIR377, MIR496, 1 more genes
    nsv4227910copy number variation1nstd166human GRCh37.p13 chr14: 101,522,569-101,525,065 , GRCh38.p12 chr14: 101,056,232-101,058,728 MIR154, MIR323B, 1 more genes
    nsv3914561copy number variation1nstd102humanPathogenic GRCh37 chr14: 95,990,744-107,287,708 , GRCh38 chr14: 95,524,407-106,879,501 , NCBI36 chr14: 95,060,497-106,358,753 MIR889, GLRX5, 517 more genes
    nsv4684265copy number variation1nstd102humanPathogenic GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456 NDUFB3P4, LINC02320, 502 more genes
    nsv3911746copy number variation1nstd102humanPathogenic GRCh38 chr14: 97,938,637-106,855,263 , GRCh37 chr14: 98,404,974-107,263,478 , NCBI36 chr14: 97,474,727-106,334,523 MIR1185-2, LOC105370685, 477 more genes
    nsv3921506copy number variation1nstd102humanPathogenic GRCh38 chr14: 99,831,655-106,855,263 , GRCh37 chr14: 100,297,992-107,263,478 , NCBI36 chr14: 99,367,745-106,334,523 RPL21P13, EXOC3L4, 453 more genes
    nsv3902723copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,661,319-107,285,437 , GRCh38.p12 chr14: 100,194,982-106,877,229 NDUFB3P4, TDRD9, 448 more genes
    nsv6291768copy number variation1nstd102humanPathogenic GRCh37 chr14: 95,871,795-102,457,523 , GRCh38.p12 chr14: 95,405,458-101,991,186 CCDC85C, MEG3, 206 more genes
    nsv3922827copy number variation1nstd102humanPathogenic GRCh38 chr14: 100,309,382-106,855,263 , GRCh37 chr14: 100,775,719-107,263,478 , NCBI36 chr14: 99,845,472-106,334,523 RNU6-1316P, MIR136, 440 more genes
    nsv3914191copy number variation1nstd102humanPathogenic NCBI36 chr14: 100,118,149-106,356,482 , GRCh38 chr14: 100,582,059-106,877,229 , GRCh37 chr14: 101,048,396-107,285,437 IGHV4-55, MIR134, 436 more genes
    nsv3918080copy number variation1nstd102humanPathogenic NCBI36 chr14: 100,344,390-106,334,523 , GRCh37 chr14: 101,274,637-107,263,478 , GRCh38 chr14: 100,808,300-106,855,263 GPR132, IGHV3-23, 427 more genes
    nsv3920123copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,729,173-102,967,034 , GRCh38 chr14: 100,262,836-102,500,697 , NCBI36 chr14: 99,798,926-102,036,787 MIR1193, SNORD114-19, 147 more genes
    nsv1398052copy number variation1nstd102humanPathogenic GRCh38 chr14: 100,806,482-101,281,031 , GRCh37 chr14: 101,272,819-101,747,368 SNORD114-31, SNORD114-28, 100 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
    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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