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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905805copy number variation1nstd209human GRCh38 chr5: 140,651,190-140,651,474 , GRCh37.p13 chr5: 140,030,775-140,031,059 IK
    nsv5723277mobile element insertion1nstd211human GRCh38 chr5: 140,651,438-140,651,438 , GRCh37.p13 chr5: 140,031,023-140,031,023 IK
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 RNA5SP195, LOC112267855, 174 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4592543copy number variation1nstd183human GRCh37 chr5: 140,025,206-140,028,055 , GRCh38.p12 chr5: 140,645,621-140,648,470 MIR3655, NDUFA2, 2 more genes
    nsv4489765mobile element insertion1nstd166human GRCh37.p13 chr5: 140,027,318-140,027,318 , GRCh38.p12 chr5: 140,647,733-140,647,733 IK, NDUFA2, 2 more genes
    nsv4455072copy number variation1nstd102humanUncertain significance GRCh37 chr5: 139,447,779-140,047,037 , GRCh38.p12 chr5: 140,068,194-140,667,452 LOC112267855, RNU4-14P, 23 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
    nsv3924309copy number variation1nstd102humanPathogenic GRCh37 chr5: 138,206,826-145,191,872 , GRCh38 chr5: 138,871,137-145,812,309 , NCBI36 chr5: 138,234,725-145,172,065 FCHSD1, LOC105378208, 183 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 RNU6-236P, FAM13B, 89 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 HNRNPA3P7, RNU6-456P, 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 UQCRQ, SNHG4, 489 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 LINC01023, CTB-99A3.1, 783 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 LOC105378993, LOC107986375, 2492 more genes
    nsv3912182copy number variation1nstd102humanLikely pathogenic NCBI36 chr5: 138,306,445-143,964,773 , GRCh37.p13 chr5: 138,278,546-143,984,580 , GRCh38.p12 chr5: 138,942,857-144,605,017 CD14, DIAPH1, 176 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 LOC105374618, HARS1, 2499 more genes
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