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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127996copy number variation1nstd186human GRCh37 chr17: 80,555,942-80,556,028 , GRCh38.p12 chr17: 82,598,066-82,598,152 FOXK2
    nsv6125734copy number variation1nstd186human GRCh37 chr17: 80,554,355-80,554,424 , GRCh38.p12 chr17: 82,596,479-82,596,548 FOXK2
    nsv5980383copy number variation1nstd102humanLikely benign GRCh37 chr17: 80,544,070-80,544,216 , GRCh38 chr17: 82,586,194-82,586,340 LOC105371942, FOXK2
    nsv5978296inversion1nstd209human GRCh38 chr17: 81,945,255-82,544,213 , GRCh37.p13 chr17: 79,903,131-80,502,089 , CD7, 29 more genes
    nsv5941538copy number variation1nstd209human GRCh38 chr17: 82,598,065-82,598,151 , GRCh37.p13 chr17: 80,555,941-80,556,027 FOXK2
    nsv5941229copy number variation1nstd209human GRCh38 chr17: 82,571,868-82,582,737 , GRCh37.p13 chr17: 80,529,744-80,540,613 FOXK2, ARL2BPP9, 1 more genes
    nsv5936869copy number variation1nstd209human GRCh38 chr17: 82,568,199-82,571,720 , GRCh37.p13 chr17: 80,526,075-80,529,596 FOXK2
    nsv5933569copy number variation1nstd209human GRCh38 chr17: 82,593,096-82,593,299 , GRCh37.p13 chr17: 80,550,972-80,551,175 FOXK2
    nsv5933429copy number variation1nstd209human GRCh38 chr17: 82,520,307-82,563,352 , GRCh37.p13 chr17: 80,478,183-80,521,228 FOXK2
    nsv5931908copy number variation1nstd209human GRCh38 chr17: 82,563,545-82,568,049 , GRCh37.p13 chr17: 80,521,421-80,525,925 FOXK2
    nsv5931028copy number variation1nstd209human GRCh38 chr17: 82,587,271-82,601,300 , GRCh37.p13 chr17: 80,545,147-80,559,176 LOC105371942, FOXK2
    nsv5930340copy number variation1nstd209human GRCh38 chr17: 82,584,184-82,585,898 , GRCh37.p13 chr17: 80,542,060-80,543,774 FOXK2, LOC105371942
    nsv5721543mobile element insertion2nstd211human GRCh38 chr17: 82,549,203-82,549,203 , GRCh37.p13 chr17: 80,507,079-80,507,079 FOXK2
    nsv5713690mobile element insertion1nstd211human GRCh38 chr17: 82,525,962-82,525,962 , GRCh37.p13 chr17: 80,483,838-80,483,838 FOXK2
    nsv5674260copy number variation1nstd102humanUncertain significance GRCh38 chr17: 82,586,979-83,257,441 , GRCh37.p13 chr17: 80,544,855-81,195,210 MIR4525, FN3K, 15 more genes
    nsv5664405insertion1nstd207human GRCh38 chr17: 82,586,308-82,586,308 , GRCh37.p13 chr17: 80,544,184-80,544,184 FOXK2, LOC105371942
    nsv5663565insertion1nstd207human GRCh38 chr17: 82,586,449-82,586,449 , GRCh37.p13 chr17: 80,544,325-80,544,325 FOXK2, LOC105371942
    nsv5663165insertion1nstd207human GRCh38 chr17: 82,586,258-82,586,258 , GRCh37.p13 chr17: 80,544,134-80,544,134 LOC105371942, FOXK2
    nsv5662710insertion1nstd207human GRCh38 chr17: 82,586,259-82,586,259 , GRCh37.p13 chr17: 80,544,135-80,544,135 FOXK2, LOC105371942
    nsv5659926insertion1nstd207human GRCh38 chr17: 82,593,155-82,593,155 , GRCh37.p13 chr17: 80,551,031-80,551,031 FOXK2
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