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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv442545copy number variation121nstd22human NCBI35 chr9: 43,806,624-43,934,502 , GRCh37.p13 chr9: 44,727,859-44,855,737 , GRCh38.p12 chr9: 61,520,021-61,647,899 LOC105379437
    nsv442532copy number variation6nstd22human NCBI35 chr8: 137,836,926-137,925,499 , GRCh37.p13 chr8: 137,767,744-137,856,317 , GRCh38.p12 chr8: 136,755,501-136,844,074 LINC02055
    nsv442616copy number variation67nstd22human NCBI35 chr11: 54,722,184-54,793,048 , GRCh37.p13 chr11: 54,965,608-55,036,472 , GRCh38.p12 chr11: 55,198,132-55,268,996 TRIM48
    nsv442991copy number variation65nstd22human NCBI35 chr6: 79,025,784-79,091,904 , GRCh37.p13 chr6: 78,969,065-79,035,185 , GRCh38.p12 chr6: 78,259,348-78,325,468 LOC105377865
    nsv442683copy number variation57nstd22human NCBI35 chr14: 40,680,246-40,727,099 , GRCh37.p13 chr14: 41,610,496-41,657,349 , GRCh38.p12 chr14: 41,141,293-41,188,146 LINC02315
    nsv442969copy number variation206nstd22human NCBI35 chr5: 177,090,005-177,131,055 , GRCh37.p13 chr5: 177,157,399-177,198,449 , GRCh38.p12 chr5: 177,730,398-177,771,448 FAM153A
    nsv442776copy number variation260nstd22human NCBI35 chr20: 1,509,580-1,541,893 , GRCh37.p13 chr20: 1,561,580-1,593,893 , GRCh38.p12 chr20: 1,580,934-1,613,247 SIRPB1
    nsv442723copy number variation78nstd22human NCBI35 chr16: 54,353,890-54,379,945 , GRCh37.p13 chr16: 55,796,389-55,822,444 , GRCh38.p12 chr16: 55,762,477-55,788,532 CES1P1
    nsv442954copy number variation6nstd22human NCBI35 chr5: 97,098,292-97,119,490 , GRCh37.p13 chr5: 97,072,536-97,093,734 , GRCh38.p12 chr5: 97,736,832-97,758,030 LOC391813
    nsv442803copy number variation170nstd22human NCBI35 chr2: 97,599,265-97,620,228 , GRCh37.p13 chr2: 98,140,747-98,161,710 , GRCh38.p12 chr2: 97,524,284-97,545,247 ANKRD36B
    nsv442671copy number variation119nstd22human NCBI35 chr13: 56,656,271-56,676,381 , GRCh37.p13 chr13: 57,758,270-57,778,380 , GRCh38.p12 chr13: 57,184,136-57,204,246 MTCO2P3
    nsv442674copy number variation15nstd22human NCBI35 chr13: 68,149,981-68,166,243 , GRCh37.p13 chr13: 69,251,980-69,268,242 , GRCh38.p12 chr13: 68,677,848-68,694,110 RN7SL761P
    nsv442238copy number variation94nstd22human NCBI35 chr7: 149,723,449-149,739,217 , GRCh37.p13 chr7: 150,285,801-150,301,569 , GRCh38.p12 chr7: 150,588,713-150,604,481 EIF2AP2
    nsv442759copy number variation270nstd22human NCBI35 chr19: 8,256,197-8,271,067 , GRCh37.p13 chr19: 8,350,197-8,365,067 , GRCh38.p12 chr19: 8,285,313-8,300,183 CD320
    nsv442294copy number variation267nstd22human NCBI35 chr7: 157,617,027-157,631,641 , GRCh37.p13 chr7: 158,117,551-158,132,165 , GRCh38.p12 chr7: 158,324,859-158,339,473 , GRCh38.p12 chr7|NT_187560.1: 137,702-152,355 PTPRN2
    nsv442150copy number variation117nstd22human NCBI35 chr7: 133,242,450-133,256,409 , GRCh37.p13 chr7: 133,785,195-133,799,154 , GRCh38.p12 chr7: 134,100,442-134,114,401
    nsv442518copy number variation92nstd22human NCBI35 chr8: 58,279,104-58,292,579 , GRCh37.p13 chr8: 58,116,550-58,130,025 , GRCh38.p12 chr8: 57,203,991-57,217,466 LINC01606
    nsv442286copy number variation134nstd22human NCBI35 chr7: 156,837,843-156,850,316 , GRCh37.p13 chr7: 157,338,367-157,350,840 , GRCh38.p12 chr7: 157,545,673-157,558,146 PTPRN2
    nsv442481copy number variation25nstd22human NCBI35 chr8: 16,306,635-16,319,032 , GRCh37.p13 chr8: 16,262,264-16,274,661 , GRCh38.p12 chr8: 16,404,755-16,417,152 LOC101929028
    nsv442936copy number variation91nstd22human NCBI35 chr5: 12,868,780-12,879,650 , GRCh37.p13 chr5: 12,815,780-12,826,650 , GRCh38.p12 chr5: 12,815,668-12,826,538 LOC105374657
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