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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137135copy number variation1nstd102humanPathogenic GRCh37 chr14: 88,401,076-94,725,706 , GRCh38.p12 chr14: 87,934,732-94,140,555 LOC100128939, FAM181A-AS1, 104 more genes
    nsv7094458copy number variation1nstd102humanPathogenic GRCh37 chr14: 88,401,064-88,406,335 , GRCh38.p12 chr14: 87,934,720-87,939,991 GALC
    nsv7094349copy number variation1nstd102humanUncertain significance GRCh37 chr14: 88,391,407-89,343,754 , GRCh38.p12 chr14: 87,925,063-88,877,410 LOC105370612, SPATA7, 15 more genes
    nsv7094270copy number variation1nstd102humanPathogenic GRCh37 chr14: 88,434,669-88,434,844 , GRCh38.p12 chr14: 87,968,325-87,968,500 GALC
    nsv7069334inversion1nstd229human GRCh38 chr14: 84,501,002-89,358,377 , GRCh37.p13 chr14: 84,967,346-89,824,721 EML5, LOC105370612, 35 more genes
    nsv7066414inversion1nstd229human GRCh38 chr14: 79,890,342-89,436,638 , GRCh37.p13 chr14: 80,356,685-89,902,982 SPATA7, RNU6ATAC28P, 82 more genes
    nsv7059378inversion1nstd229human GRCh38 chr14: 87,626,566-93,230,083 , GRCh37.p13 chr14: 88,092,910-93,674,575 PSMC1, HISLA, 87 more genes
    nsv6974955copy number variation1nstd229human GRCh38 chr14: 87,934,034-87,934,396 , GRCh37.p13 chr14: 88,400,378-88,400,740 GALC
    nsv6973525copy number variation1nstd229human GRCh38 chr14: 87,943,655-88,224,918 , GRCh37.p13 chr14: 88,409,999-88,691,262 GALC, KCNK10, 7 more genes
    nsv6972108copy number variation1nstd229human GRCh38 chr14: 87,976,201-87,980,400 , GRCh37.p13 chr14: 88,442,545-88,446,744 GALC
    nsv6968285copy number variation1nstd229human GRCh38 chr14: 87,947,693-87,948,159 , GRCh37.p13 chr14: 88,414,037-88,414,503 GALC
    nsv6967952copy number variation1nstd229human GRCh38 chr14: 87,945,178-87,960,235 , GRCh37.p13 chr14: 88,411,522-88,426,579 SHLD2P2, GALC
    nsv6967834copy number variation1nstd229human GRCh38 chr14: 87,963,331-87,974,622 , GRCh37.p13 chr14: 88,429,675-88,440,966 GALC
    nsv6966308copy number variation1nstd229human GRCh38 chr14: 87,925,162-87,956,828 , GRCh37.p13 chr14: 88,391,506-88,423,172 GALC, SHLD2P2
    nsv6966028copy number variation1nstd229human GRCh38 chr14: 87,992,801-87,998,800 , GRCh37.p13 chr14: 88,459,145-88,465,144 GALC, RNU6-835P
    nsv6965983copy number variation1nstd229human GRCh38 chr14: 87,990,701-87,995,200 , GRCh37.p13 chr14: 88,457,045-88,461,544 GALC, RNU6-835P
    nsv6965654copy number variation1nstd229human GRCh38 chr14: 87,932,268-87,977,246 , GRCh37.p13 chr14: 88,398,612-88,443,590 SHLD2P2, GALC
    nsv6965583copy number variation1nstd229human GRCh38 chr14: 87,974,086-87,977,949 , GRCh37.p13 chr14: 88,440,430-88,444,293 GALC
    nsv6965504copy number variation1nstd229human GRCh38 chr14: 87,982,179-88,164,542 , GRCh37.p13 chr14: 88,448,523-88,630,886 GALC, GPR65, 5 more genes
    nsv6961761copy number variation1nstd229human GRCh38 chr14: 87,965,629-87,973,104 , GRCh37.p13 chr14: 88,431,973-88,439,448 GALC
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