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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148227copy number variation1nstd102humanPathogenic GRCh38 chr14: 102,263,440-106,874,929 , GRCh37.p13 chr14: 102,729,777-107,283,138 TNFAIP2, IGHV4-30-2, 306 more genes
    nsv7137201copy number variation1nstd102humanPathogenic GRCh37 chr14: 103,636,647-107,285,437 , GRCh38.p12 chr14: 103,170,310-106,877,229 IGHD, IGH, 281 more genes
    nsv7094487copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,850,747-105,956,197 , GRCh38.p12 chr14: 105,384,410-105,489,860 TEX22, MTA1-DT, 5 more genes
    nsv7071453inversion1nstd229human GRCh38 chr14: 104,922,043-106,758,290 , GRCh37.p13 chr14: 105,388,380-106,929,356 , GRCh37.p13 chr14|NW_004166863.1: 1-1,421,457 IGHD1-14, IGHVII-53-1, 206 more genes
    nsv7070604inversion1nstd229human GRCh38 chr14: 105,370,034-105,412,452 , GRCh37.p13 chr14|NW_004166863.1: 33,201-75,619 , GRCh37.p13 chr14: 105,836,371-105,878,789 PACS2, RPS20P33, 1 more genes
    nsv7064632inversion1nstd229human GRCh38 chr14: 105,370,035-105,415,921 , GRCh37.p13 chr14: 105,836,372-105,882,258 , GRCh37.p13 chr14|NW_004166863.1: 33,202-79,088 PACS2, TEX22, 2 more genes
    nsv6975352copy number variation1nstd229human GRCh38 chr14: 105,394,532-105,397,606 , GRCh37.p13 chr14|NW_004166863.1: 57,699-60,773 , GRCh37.p13 chr14: 105,860,869-105,863,943 TEX22, PACS2
    nsv6973451copy number variation1nstd229human GRCh38 chr14: 105,406,694-105,438,896 , GRCh37.p13 chr14|NW_004166863.1: 69,861-102,063 , GRCh37.p13 chr14: 105,873,031-105,905,233 TEX22, MTA1, 1 more genes
    nsv6971052copy number variation1nstd229human GRCh38 chr14: 105,395,862-105,406,914 , GRCh37.p13 chr14: 105,862,199-105,873,251 , GRCh37.p13 chr14|NW_004166863.1: 59,029-70,081 PACS2, TEX22
    nsv6970767copy number variation1nstd229human GRCh38 chr14: 105,314,723-105,413,082 , GRCh37.p13 chr14|NW_004166863.1: 1-76,249 , GRCh37.p13 chr14: 105,803,171-105,879,419 RPS20P33, TEX22, 2 more genes
    nsv6968078copy number variation1nstd229human GRCh38 chr14: 105,409,579-105,417,181 , GRCh37.p13 chr14|NW_004166863.1: 72,746-80,348 , GRCh37.p13 chr14: 105,875,916-105,883,518 TEX22, MTA1-DT
    nsv6965009copy number variation1nstd229human GRCh38 chr14: 105,395,861-105,399,828 , GRCh37.p13 chr14|NW_004166863.1: 59,028-62,995 , GRCh37.p13 chr14: 105,862,198-105,866,165 TEX22, PACS2
    nsv6964179copy number variation1nstd229human GRCh38 chr14: 105,369,501-105,415,900 , GRCh37.p13 chr14|NW_004166863.1: 32,668-79,067 , GRCh37.p13 chr14: 105,835,838-105,882,237 MTA1-DT, PACS2, 2 more genes
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6622438copy number variation1nstd224human GRCh37 chr14: 105,773,028-107,287,663 , GRCh38.p12 chr14: 105,306,691-106,879,456 , GRCh38.p12 chr14|NT_187600.1: 1-1,214,078 CRIP2, BRF1, 214 more genes
    nsv6586818inversion1nstd223human GRCh37.p13 chr14|NW_004166863.1: 33,201-75,619 , GRCh38 chr14: 105,370,034-105,412,452 , GRCh37.p13 chr14: 105,836,371-105,878,789 PACS2, TEX22, 1 more genes
    nsv6515306copy number variation1nstd223human GRCh38 chr14: 105,412,242-105,415,920 , GRCh37.p13 chr14: 105,878,579-105,882,257 , GRCh37.p13 chr14|NW_004166863.1: 75,409-79,087 MTA1-DT, TEX22
    nsv6512614copy number variation1nstd223human GRCh38 chr14: 105,403,320-105,403,661 , GRCh37.p13 chr14|NW_004166863.1: 66,487-66,828 , GRCh37.p13 chr14: 105,869,657-105,869,998 TEX22
    nsv6512067copy number variation1nstd223human GRCh38 chr14: 105,406,694-105,438,896 , GRCh37.p13 chr14: 105,873,031-105,905,233 , GRCh37.p13 chr14|NW_004166863.1: 69,861-102,063 TEX22, MTA1, 1 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
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