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Items: 1 to 20 of 23

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096752copy number variation1nstd102humanUncertain significance GRCh37 chr5: 137,515,370-137,523,102 , GRCh38.p12 chr5: 138,179,681-138,187,413 KIF20A, CDC23
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 KIF20A, MEGF10, 2080 more genes
    nsv3884357copy number variation2nstd102humanPathogenic GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440 KIF20A, TXNDC15, 962 more genes
    nsv3912937copy number variation1nstd102humanPathogenic GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387 KIF20A, LINC01023, 783 more genes
    nsv6313595copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,031,902-137,623,639 , GRCh38.p12 chr5: 132,696,210-138,287,950 KIF20A, TGFBI, 110 more genes
    nsv3919979copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,737,257-137,772,727 , GRCh38 chr5: 133,401,565-138,437,038 , NCBI36 chr5: 132,765,156-137,800,626 KIF20A, FBXL21P, 92 more genes
    nsv5381777copy number variation1nstd102humanPathogenic GRCh37 chr5: 136,409,875-137,739,167 , GRCh38.p12 chr5: 137,074,186-138,403,478 KIF20A, HNRNPA0, 24 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 KIF20A, LOC105374618, 2499 more genes
    nsv3871533copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343 KIF20A, PCDHGC5, 2492 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 KIF20A, SPEF2, 2490 more genes
    nsv3874238copy number variation1nstd102humanPathogenic GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337 KIF20A, PJA2, 1228 more genes
    nsv3878636copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,125,085-157,574,910 , GRCh38.p12 chr5: 130,789,392-158,147,902 KIF20A, LOC100288484, 551 more genes
    nsv3923414copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811 KIF20A, HNRNPA3P7, 514 more genes
    nsv3914009copy number variation1nstd102humanPathogenic NCBI36 chr5: 129,211,386-152,713,299 , GRCh38 chr5: 129,847,794-153,353,546 , GRCh37 chr5: 129,183,487-152,733,106 KIF20A, UQCRQ, 489 more genes
    nsv3910250copy number variation1nstd102humanPathogenic GRCh38 chr5: 135,297,294-140,106,003 , GRCh37 chr5: 134,632,984-139,485,588 , NCBI36 chr5: 134,660,883-139,465,772 KIF20A, SNORD63, 94 more genes
    nsv3923450copy number variation1nstd102humanPathogenic GRCh37 chr5: 137,172,371-140,075,946 , NCBI36 chr5: 137,200,270-140,056,130 , GRCh38 chr5: 137,836,682-140,696,361 KIF20A, RNU6-236P, 89 more genes
    nsv3884275copy number variation1nstd102humanLikely benign GRCh37 chr5: 94,844,077-178,830,410 , GRCh38.p12 chr5: 95,508,373-179,403,409 KIF20A, LOC107986368, 1258 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 KIF20A, RNU1-150P, 1757 more genes
    nsv7097022copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-138,861,289 , GRCh38.p12 chr5: 137,622,098-139,481,704 KIF20A, CDC25C, 55 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 KIF20A, LOC105378993, 2492 more genes
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