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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv4944622copy number variation1nstd200human GRCh38 chr5: 38,693,304-38,793,720 , GRCh37.p13 chr5: 38,693,406-38,793,822 LOC100132789, LINC01265, 2 more genes
    nsv4680426copy number variation1nstd189human GRCh37.p13 chr5: 37,623,394-42,403,769 , GRCh38.p12 chr5: 37,623,292-42,403,667 , C6, 65 more genes
    nsv4674231copy number variation1nstd102humanPathogenic GRCh37 chr5: 38,432,180-49,441,945 , GRCh38.p12 chr5: 38,432,078-50,146,111 RPSAP38, LOC105374746, 92 more genes
    nsv4456866copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,453,883-46,389,339 , GRCh38.p12 chr5: 34,453,778-46,389,237 LOC100506639, EEF1A1P19, 146 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
    nsv4322917inversion1nstd166human GRCh37.p13 chr5: 37,539,888-43,176,744 , GRCh38.p12 chr5: 37,539,786-43,176,642 , PTGER4, 86 more genes
    nsv4127150copy number variation1nstd166human GRCh37.p13 chr5: 38,716,746-38,717,939 , GRCh38.p12 chr5: 38,716,644-38,717,837 LINC01265, OSMR-DT
    nsv3924942copy number variation1nstd102humanPathogenic GRCh37 chr5: 37,016,145-39,383,383 , GRCh38 chr5: 37,016,043-39,383,281 , NCBI36 chr5: 37,051,902-39,419,140 LINC02119, WDR70, 38 more genes
    nsv3923992copy number variation1nstd102humanPathogenic GRCh37 chr5: 50,093-46,115,086 , NCBI36 chr5: 103,093-46,150,843 , GRCh38 chr5: 49,978-46,114,984 LOC100130748, CDH10, 533 more genes
    nsv3920978copy number variation1nstd102humanLikely benign NCBI36 chr5: 38,577,981-38,796,787 , GRCh37 chr5: 38,542,224-38,761,030 , GRCh38 chr5: 38,542,122-38,760,928 LIFR-AS1, OSMR-DT, 4 more genes
    nsv3920391copy number variation1nstd102humanPathogenic GRCh38 chr5: 35,201,559-61,903,141 , GRCh37 chr5: 35,201,661-61,198,968 , NCBI36 chr5: 35,237,418-61,234,725 KRT18P56, LINC01265, 290 more genes
    nsv3917947copy number variation1nstd102humanPathogenic GRCh38 chr5: 35,700,480-45,260,029 , NCBI36 chr5: 35,736,339-45,295,888 , GRCh37 chr5: 35,700,582-45,260,131 LINC02104, LOC100132789, 134 more genes
    nsv3916709copy number variation1nstd102humanPathogenic GRCh37 chr5: 36,374,209-50,399,675 , NCBI36 chr5: 36,409,966-50,435,432 , GRCh38 chr5: 36,374,107-51,103,841 SLC1A3-AS1, LOC105374745, 126 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
    nsv3911585copy number variation1nstd102humanPathogenic NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550 LINC02241, ATPSCKMT, 878 more genes
    nsv3911295copy number variation1nstd102humanPathogenic GRCh37 chr5: 54,954-45,649,963 , NCBI36 chr5: 107,954-45,685,720 , GRCh38 chr5: 54,839-45,649,861 PMCHL1, LINC02211, 532 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
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