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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv442779copy number variation41nstd22human NCBI35 chr20: 28,034,013-28,119,552 , GRCh37.p13 chr20: 29,420,352-29,505,891 , GRCh38.p12 chr20: 30,185,676-30,271,215 CFTRP3
    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
    nsv442908copy number variation238nstd22human NCBI35 chr1: 72,480,937-72,523,169 , GRCh37.p13 chr1: 72,768,916-72,811,148 , GRCh38.p12 chr1: 72,303,233-72,345,465 , GRCh38.p12 chr1|NW_018654707.1: 15,500-66,690 LOC105378797
    nsv442901copy number variation79nstd22human NCBI35 chr4: 34,601,591-34,646,749 , GRCh37.p13 chr4|NW_003315915.1: 269,732-314,890 , GRCh37.p13 chr4: 34,779,025-34,824,183 , GRCh38.p12 chr4: 34,777,403-34,822,561 , GRCh38.p12 chr4|NW_003315915.1: 269,732-314,890 LOC105378262
    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
    nsv442690copy number variation115nstd22human NCBI35 chr15: 22,029,857-22,065,565 , GRCh37.p13 chr15: 24,478,764-24,514,472 , GRCh38.p12 chr15: 24,233,617-24,269,325 LOC105370733
    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
    nsv442187copy number variation52nstd22human NCBI35 chr7: 141,222,827-141,245,092 , GRCh37.p13 chr7|NW_003571040.1: 211,794-234,059 , GRCh37.p13 chr7: 141,769,643-141,791,908 , GRCh38.p12 chr7: 142,069,843-142,092,108 , GRCh38.p12 chr7|NT_187562.1: 31,723-53,988 MGAM
    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
    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
    nsv442730copy number variation99nstd22human NCBI35 chr16: 76,929,941-76,942,266 , GRCh37.p13 chr16: 78,372,440-78,384,765 , GRCh38.p12 chr16: 78,338,543-78,350,868 WWOX
    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
    nsv442782copy number variation156nstd22human NCBI35 chr2: 87,426,037-87,434,600 , GRCh37.p13 chr2: 87,514,379-87,522,942 , GRCh38.p12 chr2: 87,287,256-87,295,819 LOC107985908
    nsv442256copy number variation163nstd22human NCBI35 chr7: 153,830,819-153,838,481 , GRCh37.p13 chr7: 154,393,171-154,400,833 , GRCh38.p12 chr7: 154,601,461-154,609,123 DPP6
    nsv441973copy number variation80nstd22human NCBI35 chr1: 149,574,996-149,581,773 , GRCh37.p13 chr1: 152,761,923-152,768,700 , GRCh38.p12 chr1: 152,789,447-152,796,224 LCE1D
    nsv442589copy number variation38nstd22human NCBI35 chr1: 219,405,720-219,411,999 , GRCh37.p13 chr1: 223,017,325-223,023,604 , GRCh38.p12 chr1: 222,843,983-222,850,262 DISP1
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