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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6312460copy number variation1nstd102humanPathogenic GRCh37 chr7: 794,206-825,290 , GRCh38.p12 chr7: 754,569-785,653 DNAAF5
    nsv6312359copy number variation1nstd102humanPathogenic GRCh37 chr7: 825,134-825,290 , GRCh38.p12 chr7: 785,497-785,653 DNAAF5
    nsv3883170copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 825,148-825,295 , GRCh38 chr7: 785,511-785,658 DNAAF5
    nsv6137689copy number variation1nstd102humanLikely benign GRCh38 chr7: 785,224-785,300 , GRCh37 chr7: 824,861-824,937 DNAAF5
    nsv6636028copy number variation1nstd102humanUncertain significance GRCh37 chr7: 824,878-824,955 , GRCh38 chr7: 785,241-785,318 DNAAF5
    nsv7097639copy number variation1nstd102humanPathogenic GRCh37 chr7: 766,358-825,290 , GRCh38.p12 chr7: 726,721-785,653 DNAAF5, PRKAR1B
    nsv7097638copy number variation1nstd102humanPathogenic GRCh37 chr7: 766,358-769,504 , GRCh38.p12 chr7: 726,721-729,867 DNAAF5, PRKAR1B
    nsv3898129copy number variation1nstd102humanUncertain significance GRCh37 chr7: 704,572-832,973 , GRCh38.p12 chr7: 664,935-793,336 DNAAF5, PRKAR1B
    nsv7098136copy number variation1nstd102humanUncertain significance GRCh37 chr7: 766,358-781,122 , GRCh38.p12 chr7: 726,721-741,485 DNAAF5, PRKAR1B
    nsv3909406copy number variation1nstd102humanUncertain significance GRCh37 chr7: 794,174-935,913 , GRCh38.p12 chr7: 754,537-896,276 DNAAF5, GET4, 2 more genes
    nsv4728852copy number variation1nstd102humanUncertain significance GRCh37 chr7: 795,826-931,003 , GRCh38.p12 chr7: 756,189-891,366 DNAAF5, SUN1, 1 more genes
    nsv3912682copy number variation1nstd102humanUncertain significance NCBI36 chr7: 695,717-861,035 , GRCh38 chr7: 689,554-854,872 , GRCh37 chr7: 729,191-894,509 DNAAF5, PRKAR1B, 1 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 DNAAF5, RNU6-438P, 2682 more genes
    nsv3920006copy number variation1nstd102humanPathogenic GRCh37 chr7: 45,130-5,920,006 , GRCh38 chr7: 45,130-5,880,375 , NCBI36 chr7: 140,213-5,886,532 DNAAF5, RNU6-215P, 120 more genes
    nsv4456136copy number variation1nstd102humanPathogenic GRCh37 chr7: 36,616-4,298,168 , GRCh38.p12 chr7: 36,616-4,258,536 DNAAF5, LOC442497, 85 more genes
    nsv3898790copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-3,642,604 , GRCh38.p12 chr7: 43,360-3,602,972 DNAAF5, RPL21P72, 83 more genes
    nsv3911664copy number variation1nstd102humanPathogenic GRCh38 chr7: 54,185-3,324,143 , GRCh37 chr7: 54,185-3,363,775 , NCBI36 chr7: 149,268-3,330,301 DNAAF5, MIR6836, 81 more genes
    nsv3912605copy number variation1nstd102humanPathogenic GRCh38 chr7: 54,165-3,258,775 , NCBI36 chr7: 149,248-3,264,933 , GRCh37 chr7: 54,165-3,298,407 DNAAF5, LOC100129603, 80 more genes
    nsv3916297copy number variation2nstd102humanPathogenic GRCh38 chr7: 54,185-1,843,584 , NCBI36 chr7: 149,268-1,849,746 , GRCh37 chr7: 54,185-1,883,220 DNAAF5, MAD1L1, 51 more genes
    nsv4675871copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-1,750,797 , GRCh38.p12 chr7: 44,935-1,711,161 DNAAF5, C7orf50, 47 more genes
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