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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5928539copy number variation1nstd209human GRCh38 chr14: 92,929,294-92,929,373 , GRCh37.p13 chr14: 93,395,639-93,395,718 CHGA
    nsv5585011copy number variation1nstd207human GRCh38 chr14: 92,929,294-92,929,373 , GRCh37.p13 chr14: 93,395,639-93,395,718 CHGA
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5007333copy number variation1nstd200human GRCh38 chr14: 92,933,351-92,934,292 , GRCh37.p13 chr14: 93,399,696-93,400,637 CHGA
    nsv5004938copy number variation1nstd200human GRCh38 chr14: 92,925,955-92,970,922 , GRCh37.p13 chr14: 93,392,300-93,437,267 CHGA, ITPK1
    nsv4863563copy number variation1nstd200human GRCh37 chr14: 93,392,300-93,437,267 , GRCh38.p12 chr14: 92,925,955-92,970,922 , GRCh38.p12 chr14|NT_187601.1: 40,517-85,484 ITPK1, CHGA
    nsv4849511copy number variation1nstd200human GRCh37 chr14: 93,399,696-93,400,637 , GRCh38.p12 chr14: 92,933,351-92,934,292 , GRCh38.p12 chr14|NT_187601.1: 47,913-48,854 CHGA
    nsv4675107copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,783,523-96,907,490 , GRCh38.p12 chr14: 84,317,179-96,441,153 SHLD2P2, RPL15P2, 175 more genes
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 LOC105370639, SERPINA9, 600 more genes
    nsv4322697inversion1nstd166human GRCh37.p13 chr14: 93,328,296-94,706,279 , GRCh38.p12 chr14: 92,861,951-94,140,555 , GRCh38.p12 chr14|NT_187601.1: 1-1,354,504 ASB2, UNC79, 29 more genes
    nsv4222110copy number variation1nstd166human GRCh37.p13 chr14: 93,392,301-93,437,266 , GRCh38.p12 chr14|NT_187601.1: 40,518-85,483 , GRCh38.p12 chr14: 92,925,956-92,970,921 CHGA, ITPK1
    nsv3922566copy number variation1nstd102humanPathogenic GRCh38 chr14: 90,255,156-95,274,696 , GRCh37 chr14: 90,721,500-95,741,033 , NCBI36 chr14: 89,791,253-94,810,786 RPSAP4, LOC105370622, 97 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
    nsv3921292copy number variation1nstd102humanPathogenic GRCh38 chr14: 91,455,861-106,832,642 , GRCh37 chr14: 91,922,205-107,240,869 , NCBI36 chr14: 90,991,958-106,311,914 IGHVII-15-1, LINC03117, 594 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
    nsv3915681copy number variation1nstd102humanPathogenic NCBI36 chr14: 76,758,891-106,358,550 , GRCh37 chr14: 77,689,138-107,287,505 , GRCh38 chr14: 77,222,795-106,879,298 IGHV3-32, SNORD114-31, 751 more genes
    nsv3914983copy number variation1nstd102humanPathogenic GRCh38 chr14: 86,094,030-106,832,642 , GRCh37 chr14: 86,560,374-107,240,869 , NCBI36 chr14: 85,630,127-106,311,914 IGHD5-5, EML5, 658 more genes
    nsv3914883copy number variation1nstd102humanPathogenic NCBI36 chr14: 92,077,081-104,401,040 , GRCh37 chr14: 93,007,328-105,329,995 , GRCh38 chr14: 92,540,983-104,863,658 LINC03117, EIF5, 360 more genes
    nsv3914418copy number variation1nstd102humanPathogenic NCBI36 chr14: 92,401,537-106,360,585 , GRCh37.p13 chr14: 93,331,784-107,289,540 , GRCh38.p12 chr14: 92,865,439-106,881,350 IGHVII-60-1, ATG2B, 582 more genes
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