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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 ZMAT2, MEGF10, 2080 more genes
    nsv3884357copy number variation2nstd102humanPathogenic GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440 ZMAT2, 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 ZMAT2, LINC01023, 783 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 ZMAT2, FCHSD1, 183 more genes
    nsv3872314copy number variation1nstd102humanPathogenic GRCh37 chr5: 139,147,238-141,540,491 , GRCh38.p12 chr5: 139,767,653-142,160,926 ZMAT2, VTRNA1-1, 122 more genes
    nsv6290261copy number variation1nstd102humanPathogenic GRCh37 chr5: 139,493,717-140,517,454 , GRCh38.p12 chr5: 140,114,132-141,137,872 ZMAT2, PCDHA2, 57 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 ZMAT2, LOC105374618, 2499 more genes
    nsv3871533copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343 ZMAT2, PCDHGC5, 2492 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 ZMAT2, SPEF2, 2490 more genes
    nsv3874238copy number variation1nstd102humanPathogenic GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337 ZMAT2, PJA2, 1228 more genes
    nsv3878636copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,125,085-157,574,910 , GRCh38.p12 chr5: 130,789,392-158,147,902 ZMAT2, 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 ZMAT2, 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 ZMAT2, UQCRQ, 489 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 ZMAT2, CD14, 176 more genes
    nsv3884275copy number variation1nstd102humanLikely benign GRCh37 chr5: 94,844,077-178,830,410 , GRCh38.p12 chr5: 95,508,373-179,403,409 ZMAT2, 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 ZMAT2, RNU1-150P, 1757 more genes
    nsv7097512copy number variation1nstd102humanUncertain significance GRCh37 chr5: 139,930,285-140,078,137 , GRCh38.p12 chr5: 140,550,700-140,698,552 ZMAT2, TMCO6, 15 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 ZMAT2, LOC105378993, 2492 more genes
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 ZMAT2, RNA5SP195, 174 more genes
    nsv7096751copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-140,078,137 , GRCh38.p12 chr5: 137,622,098-140,698,552 ZMAT2, CDC25C, 94 more genes
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