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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095062copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,556,653-89,851,392 , GRCh38.p12 chr16: 89,490,245-89,784,984 SNORD68, CHMP1A, 15 more genes
    nsv7095060copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,167,090-89,883,023 , GRCh38.p12 chr16: 89,100,682-89,816,615 VPS9D1, ZNF276, 26 more genes
    nsv7094940copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,611,036-90,106,937 , GRCh38.p12 chr16: 89,544,628-90,040,529 SPATA2L, LINC02166, 25 more genes
    nsv7094939copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,371,594-89,730,828 , GRCh38.p12 chr16: 89,305,186-89,664,420 LOC101930112, LOC101927863, 12 more genes
    nsv7094704copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,334,886-89,723,996 , GRCh38.p12 chr16: 89,268,478-89,657,588 LOC101930112, LOC101927863, 13 more genes
    nsv7094699copy number variation2nstd102humanUncertain significance GRCh37 chr16: 87,636,753-90,109,753 , GRCh38.p12 chr16: 87,603,147-90,043,345 HSALR1, LOC105371412, 87 more genes
    nsv7094617copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,574,826-89,583,809 , GRCh38.p12 chr16: 89,508,418-89,517,401 SPG7
    nsv7073763inversion1nstd229human GRCh38 chr16: 89,536,886-89,757,402 , GRCh37.p13 chr16: 89,603,294-89,823,810 SPATA33, SNORD68, 12 more genes
    nsv6996366copy number variation1nstd229human GRCh38 chr16: 89,352,857-89,508,759 , GRCh37.p13 chr16: 89,419,265-89,575,167 LOC101927817, CMPK1P2, 5 more genes
    nsv6995211copy number variation1nstd229human GRCh38 chr16: 89,417,001-89,678,600 , GRCh37.p13 chr16: 89,483,409-89,745,008 LOC101927817, CPNE7, 11 more genes
    nsv6994168copy number variation1nstd229human GRCh38 chr16: 89,537,372-89,550,181 , GRCh37.p13 chr16: 89,603,780-89,616,589 SPG7
    nsv6992944copy number variation1nstd229human GRCh38 chr16: 89,301,591-89,661,186 , GRCh37.p13 chr16: 89,367,999-89,727,594 CMPK1P2, LOC101927863, 12 more genes
    nsv6991511copy number variation1nstd229human GRCh38 chr16: 89,532,677-89,552,541 , GRCh37.p13 chr16: 89,599,085-89,618,949 SPG7
    nsv6991055copy number variation1nstd229human GRCh38 chr16: 89,543,818-89,544,327 , GRCh37.p13 chr16: 89,610,226-89,610,735 SPG7
    nsv6988032copy number variation1nstd229human GRCh38 chr16: 89,535,627-89,537,991 , GRCh37.p13 chr16: 89,602,035-89,604,399 SPG7
    nsv6985866copy number variation1nstd229human GRCh38 chr16: 89,473,541-89,719,269 , GRCh37.p13 chr16: 89,539,949-89,785,677 ANKRD11, SPATA33, 14 more genes
    nsv6985799copy number variation1nstd229human GRCh38 chr16: 89,521,401-89,540,100 , GRCh37.p13 chr16: 89,587,809-89,606,508 SPG7
    nsv6984474copy number variation1nstd229human GRCh38 chr16: 89,505,104-89,515,967 , GRCh37.p13 chr16: 89,571,512-89,582,375 SPG7
    nsv6982368copy number variation1nstd229human GRCh38 chr16: 89,515,114-89,543,413 , GRCh37.p13 chr16: 89,581,522-89,609,821 SPG7
    nsv6981781copy number variation1nstd229human GRCh38 chr16: 89,525,127-89,525,157 , GRCh37.p13 chr16: 89,591,535-89,591,565 SPG7
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