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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4676362copy number variation1nstd102humanUncertain significance GRCh37 chr18: 59,071,708-59,281,636 , GRCh38.p12 chr18: 61,404,475-61,614,403 CDH20, RPL30P14
    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
    nsv3884357copy number variation2nstd102humanPathogenic GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440 TXNDC15, PCDHAC1, 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 LINC01023, CTB-99A3.1, 783 more genes
    nsv3902831copy number variation1nstd102humanPathogenic GRCh37 chr18: 46,177,798-78,014,123 , GRCh38.p12 chr18: 48,651,427-80,256,240 CDH20, LOC105372180, 370 more genes
    nsv3906152copy number variation1nstd102humanPathogenic GRCh37 chr18: 46,942,427-78,014,123 , GRCh38.p12 chr18: 49,416,057-80,256,240 CDH20, RPL17P44, 360 more genes
    nsv3909519copy number variation1nstd102humanPathogenic GRCh37 chr18: 47,656,799-78,014,123 , GRCh38.p12 chr18: 50,130,429-80,256,240 CDH20, 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 CDH20, 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 CDH20, LOC105372200, 319 more genes
    nsv4676105copy number variation1nstd102humanPathogenic GRCh37 chr18: 49,460,596-78,014,123 , GRCh38.p12 chr18: 51,934,226-80,256,240 CDH20, 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 CDH20, 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 CDH20, NETO1, 303 more genes
    nsv6314216copy number variation1nstd102humanPathogenic GRCh37 chr18: 52,675,201-78,014,123 , GRCh38.p12 chr18: 55,007,970-80,256,240 CDH20, RNA5SP461, 290 more genes
    nsv3899425copy number variation1nstd102humanPathogenic GRCh37 chr18: 52,802,515-78,015,180 , GRCh38.p12 chr18: 55,135,284-80,257,297 CDH20, 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 CDH20, LOC102725148, 287 more genes
    nsv3903916copy number variation1nstd102humanPathogenic GRCh37 chr18: 52,837,852-77,989,426 , GRCh38.p12 chr18: 55,170,621-80,231,543 CDH20, CBLN2, 287 more genes
    nsv3900769copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,100,584-78,014,123 , GRCh38.p12 chr18: 55,433,353-80,256,240 CDH20, LOC105372130, 287 more genes
    nsv6314188copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,309,113-78,014,123 , GRCh38.p12 chr18: 55,641,882-80,256,240 CDH20, 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 CDH20, 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 CDH20, LINC02565, 272 more genes
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