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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3890590copy number variation1nstd102humanBenign GRCh37 chr18: 72,974,307-73,015,984 , GRCh38.p12 chr18: 75,262,352-75,304,029 TSHZ1
    nsv3901121copy number variation1nstd102humanUncertain significance GRCh37 chr18: 72,620,754-72,935,461 , GRCh38.p12 chr18: 74,908,798-75,223,506 TSHZ1, LOC105376874, 2 more genes
    nsv4676351copy number variation1nstd102humanUncertain significance GRCh37 chr18: 72,933,453-73,215,883 , GRCh38.p12 chr18: 75,221,498-75,503,928 TSHZ1, LOC105372201, 3 more genes
    nsv3896982copy number variation1nstd102humanUncertain significance GRCh37 chr18: 72,799,720-73,028,198 , GRCh38.p12 chr18: 75,087,764-75,316,243 TSHZ1, PTGR3, 1 more genes
    nsv3902831copy number variation1nstd102humanPathogenic GRCh37 chr18: 46,177,798-78,014,123 , GRCh38.p12 chr18: 48,651,427-80,256,240 TSHZ1, LOC105372180, 370 more genes
    nsv3906152copy number variation1nstd102humanPathogenic GRCh37 chr18: 46,942,427-78,014,123 , GRCh38.p12 chr18: 49,416,057-80,256,240 TSHZ1, RPL17P44, 360 more genes
    nsv3909519copy number variation1nstd102humanPathogenic GRCh37 chr18: 47,656,799-78,014,123 , GRCh38.p12 chr18: 50,130,429-80,256,240 TSHZ1, LOC105372160, 339 more genes
    nsv3920508copy number variation1nstd102humanPathogenic GRCh38 chr18: 51,167,159-80,256,240 , GRCh37 chr18: 48,693,529-78,014,123 , NCBI36 chr18: 46,947,527-76,115,097 TSHZ1, LOC105372152, 319 more genes
    nsv3916196copy number variation1nstd102humanPathogenic GRCh37 chr18: 48,716,799-78,010,032 , GRCh38 chr18: 51,190,429-80,252,149 , NCBI36 chr18: 46,970,797-76,111,023 TSHZ1, LOC105372200, 319 more genes
    nsv4676105copy number variation1nstd102humanPathogenic GRCh37 chr18: 49,460,596-78,014,123 , GRCh38.p12 chr18: 51,934,226-80,256,240 TSHZ1, MIR548AV, 310 more genes
    nsv3914571copy number variation1nstd102humanPathogenic GRCh37 chr18: 49,947,422-78,012,829 , NCBI36 chr18: 48,201,420-76,113,817 , GRCh38 chr18: 52,421,052-80,254,946 TSHZ1, RPS2P6, 308 more genes
    nsv3918507copy number variation1nstd102humanPathogenic GRCh38 chr18: 53,865,057-80,252,149 , GRCh37 chr18: 51,391,427-78,010,032 , NCBI36 chr18: 49,645,425-76,111,023 TSHZ1, NETO1, 303 more genes
    nsv6314216copy number variation1nstd102humanPathogenic GRCh37 chr18: 52,675,201-78,014,123 , GRCh38.p12 chr18: 55,007,970-80,256,240 TSHZ1, RNA5SP461, 290 more genes
    nsv3899425copy number variation1nstd102humanPathogenic GRCh37 chr18: 52,802,515-78,015,180 , GRCh38.p12 chr18: 55,135,284-80,257,297 TSHZ1, ZNF236-DT, 288 more genes
    nsv3918008copy number variation1nstd102humanPathogenic GRCh37 chr18: 52,846,595-78,012,829 , GRCh38 chr18: 55,179,364-80,254,946 , NCBI36 chr18: 50,997,593-76,113,817 TSHZ1, LOC102725148, 287 more genes
    nsv3903916copy number variation1nstd102humanPathogenic GRCh37 chr18: 52,837,852-77,989,426 , GRCh38.p12 chr18: 55,170,621-80,231,543 TSHZ1, CBLN2, 287 more genes
    nsv3900769copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,100,584-78,014,123 , GRCh38.p12 chr18: 55,433,353-80,256,240 TSHZ1, LOC105372130, 287 more genes
    nsv6314188copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,309,113-78,014,123 , GRCh38.p12 chr18: 55,641,882-80,256,240 TSHZ1, ZNF236-DT, 282 more genes
    nsv6637467copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,624,405-78,014,123 , GRCh38.p12 chr18: 55,957,174-80,256,240 TSHZ1, RPL9P31, 277 more genes
    nsv3919243copy number variation1nstd102humanPathogenic GRCh38 chr18: 56,353,040-80,209,986 , GRCh37 chr18: 54,020,271-77,967,869 , NCBI36 chr18: 52,171,269-76,068,860 TSHZ1, LINC02565, 272 more genes
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