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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3897523copy number variation1nstd102humanBenign GRCh37 chr8: 68,137,315-68,161,638 , GRCh38.p12 chr8: 67,225,080-67,249,403 ARFGEF1
    nsv3907300copy number variation1nstd102humanBenign GRCh37 chr8: 68,158,038-68,161,638 , GRCh38.p12 chr8: 67,245,803-67,249,403 ARFGEF1
    nsv3909298copy number variation1nstd102humanUncertain significance GRCh37 chr8: 68,174,995-68,230,922 , GRCh38.p12 chr8: 67,262,760-67,318,687 ARFGEF1
    nsv7098985copy number variation1nstd102humanUncertain significance GRCh37 chr8: 68,115,487-68,131,665 , GRCh38.p12 chr8: 67,203,252-67,219,430 ARFGEF1
    nsv4682109copy number variation1nstd102humanUncertain significance GRCh37 chr8: 68,395,983-68,397,044 , GRCh38.p12 chr8: 67,483,748-67,484,809 CPA6, ARFGEF1-DT
    nsv6312734copy number variation1nstd102humanUncertain significance GRCh37 chr8: 68,105,679-68,105,857 , GRCh38.p12 chr8: 67,193,444-67,193,622 ARFGEF1, CSPP1
    nsv4681034copy number variation1nstd102humanUncertain significance GRCh37 chr8: 68,105,699-68,105,837 , GRCh38.p12 chr8: 67,193,464-67,193,602 ARFGEF1, CSPP1
    nsv4683581copy number variation1nstd102humanUncertain significance GRCh37 chr8: 68,334,719-68,346,495 , GRCh38.p12 chr8: 67,422,484-67,434,260 ARFGEF1-DT, CPA6
    nsv7137000copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,109,883-68,255,913 , GRCh38.p12 chr8: 67,197,648-67,343,678 ARFGEF1, CSPP1, 1 more genes
    nsv6314555complex chromosomal rearrangement7nstd102humanPathogenic GRCh37 chr8: 65,187,723-65,187,723 , GRCh37 chr8: 68,393,835-68,393,835 , GRCh37 chr8: 65,187,602-65,187,602 , GRCh37 chr8: 68,393,684-68,393,684 , GRCh37 chr8: 70,181,445-70,181,445 , GRCh37 chr8: 70,181,450-70,181,450 , GRCh37 chr8: 54,482,780-54,482,780 , GRCh37 chr8: 54,482,780-54,482,780 , GRCh37 chr10: 2,187,369-2,187,369 , GRCh37 chr10: 2,059,927-2,059,927 , GRCh37 chr10: 2,059,928-2,059,928 , GRCh37 chr10: 9,592,748-9,592,748 , GRCh37 chr10: 9,592,706-9,592,706 , GRCh37 chr10: 2,187,182-2,187,182 , GRCh38.p12 chr10: 2,017,734-2,017,734 , GRCh38.p12 chr10: 2,144,988-2,144,988 , GRCh38.p12 chr10: 9,550,785-9,550,785 , GRCh38.p12 chr10: 2,145,175-2,145,175 , GRCh38.p12 chr10: 9,550,743-9,550,743 , GRCh38.p12 chr10: 2,017,733-2,017,733 , GRCh38.p12 chr8: 64,275,045-64,275,045 , GRCh38.p12 chr8: 67,481,449-67,481,449 , GRCh38.p12 chr8: 67,481,600-67,481,600 , GRCh38.p12 chr8: 69,269,210-69,269,210 , GRCh38.p12 chr8: 69,269,215-69,269,215 , GRCh38.p12 chr8: 64,275,166-64,275,166 , GRCh38.p12 chr8: 53,570,220-53,570,220 , GRCh38.p12 chr8: 53,570,220-53,570,220 LINC02663, ARFGEF1-DT, 2 more genes
    nsv3908771copy number variation1nstd102humanUncertain significance GRCh37 chr8: 68,399,660-68,474,594 , GRCh38.p12 chr8: 67,487,425-67,562,359 CPA6, ARFGEF1-DT, 1 more genes
    nsv3890503copy number variation1nstd102humanUncertain significance GRCh37 chr8: 68,038,759-68,245,969 , GRCh38.p12 chr8: 67,126,524-67,333,734 ARFGEF1, NPM1P44, 1 more genes
    nsv3923743copy number variation1nstd102humanUncertain significance NCBI36 chr8: 68,168,381-68,307,607 , GRCh37.p13 chr8: 68,005,827-68,145,053 , GRCh38.p12 chr8: 67,093,592-67,232,818 ARFGEF1, RNA5SP268, 2 more genes
    nsv4683049copy number variation1nstd102humanUncertain significance GRCh37 chr8: 68,024,207-68,130,373 , GRCh38.p12 chr8: 67,111,972-67,218,138 ARFGEF1, CSPP1, 1 more genes
    nsv3879757copy number variation1nstd102humanUncertain significance GRCh38 chr8: 67,111,952-67,195,613 , GRCh37 chr8: 68,024,187-68,107,848 ARFGEF1, CSPP1, 1 more genes
    nsv6312650copy number variation1nstd102humanUncertain significance GRCh37 chr8: 68,024,187-68,107,828 , GRCh38.p12 chr8: 67,111,952-67,195,593 ARFGEF1, NPM1P44, 1 more genes
    nsv5381559copy number variation1nstd102humanUncertain significance GRCh37 chr8: 68,024,197-68,107,828 , GRCh38.p12 chr8: 67,111,962-67,195,593 ARFGEF1, NPM1P44, 1 more genes
    nsv3914262copy number variation1nstd102humanPathogenic GRCh37 chr8: 63,143,195-74,140,021 , GRCh38 chr8: 62,230,636-73,227,786 , NCBI36 chr8: 63,305,749-74,302,575 ARFGEF1, RRS1, 151 more genes
    nsv6290731copy number variation1nstd102humanPathogenic GRCh37 chr8: 66,045,954-69,807,260 , GRCh38.p12 chr8: 65,133,719-68,895,025 ARFGEF1, LINC00967, 64 more genes
    nsv3891386copy number variation1nstd102humanPathogenic GRCh37 chr8: 65,194,424-68,570,319 , GRCh38.p12 chr8: 64,281,867-67,658,084 ARFGEF1, MTATP6P12, 66 more genes
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