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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3891712copy number variation1nstd102humanBenign GRCh37 chr11: 85,431,954-85,473,883 , GRCh38.p12 chr11: 85,720,911-85,762,840 SYTL2
    nsv3892435copy number variation1nstd102humanBenign GRCh37 chr11: 85,431,904-85,470,893 , GRCh38.p12 chr11: 85,720,861-85,759,850 SYTL2
    nsv3890180copy number variation1nstd102humanBenign GRCh37 chr11: 85,431,954-85,470,893 , GRCh38.p12 chr11: 85,720,911-85,759,850 SYTL2
    nsv3892044copy number variation1nstd102humanBenign GRCh37 chr11: 85,432,393-85,470,893 , GRCh38.p12 chr11: 85,721,350-85,759,850 SYTL2
    nsv3907108copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,436,871-85,459,435 , GRCh38.p12 chr11: 85,725,828-85,748,392 SYTL2
    nsv3898558copy number variation1nstd102humanLikely benign GRCh37 chr11: 85,365,100-85,459,435 , GRCh38.p12 chr11: 85,654,056-85,748,392 SYTL2, TMEM126A, 2 more genes
    nsv3908642copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,475,317-85,681,916 , GRCh38.p12 chr11: 85,764,274-85,970,873 SYTL2, CCDC83, 3 more genes
    nsv6637842copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,446,871-85,629,741 , GRCh38.p12 chr11: 85,735,828-85,918,698 SYTL2, CCDC83, 1 more genes
    nsv4729498copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,452,186-85,595,636 , GRCh38.p12 chr11: 85,741,143-85,884,593 SYTL2, CCDC83, 1 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 SYTL2, FAUP4, 2031 more genes
    nsv3904761copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514 SYTL2, RPS6P16, 449 more genes
    nsv3913977copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356 SYTL2, PLS1P1, 349 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 SYTL2, LOC107984375, 295 more genes
    nsv3921121copy number variation1nstd102humanPathogenic GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688 SYTL2, LOC105369441, 296 more genes
    nsv6313961copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717 SYTL2, MTND5P38, 252 more genes
    nsv3922508copy number variation1nstd102humanPathogenic GRCh38 chr11: 85,242,847-102,920,097 , GRCh37 chr11: 84,953,891-102,738,968 , NCBI36 chr11: 84,631,539-102,296,037 SYTL2, AMOTL1, 240 more genes
    nsv3897292copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,318,996-96,116,221 , GRCh38.p12 chr11: 80,607,952-96,383,057 SYTL2, FAM181B, 218 more genes
    nsv3901209copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,771,852-90,851,187 , GRCh38.p12 chr11: 82,060,810-91,118,019 SYTL2, RPL7AP54, 124 more genes
    nsv6637847copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,562,738-88,663,067 , GRCh38.p12 chr11: 80,851,695-88,929,899 SYTL2, PRSS23, 92 more genes
    nsv4674839copy number variation1nstd102humanPathogenic GRCh37 chr11: 83,530,179-87,059,742 , GRCh38.p12 chr11: 83,819,136-87,348,700 SYTL2, PICALM, 44 more genes
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