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Items: 1 to 20 of 155

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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
    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
    nsv442859copy number variation75nstd22human NCBI35 chr3: 46,776,821-46,824,285 , GRCh37.p13 chr3: 46,801,817-46,849,281 , GRCh38.p12 chr3: 46,760,327-46,807,791 PRSS44P
    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
    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
    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
    nsv442603copy number variation8nstd22human NCBI35 chr11: 21,149,965-21,166,513 , GRCh37.p13 chr11: 21,193,389-21,209,937 , GRCh38.p12 chr11: 21,171,843-21,188,391 NELL1
    nsv442845copy number variation37nstd22human NCBI35 chr2: 203,121,281-203,137,707 , GRCh37.p13 chr2: 203,295,775-203,312,201 , GRCh38.p12 chr2: 202,431,052-202,447,478 BMPR2
    nsv441983copy number variation113nstd22human NCBI35 chr7: 66,073,479-66,089,382 , GRCh37.p13 chr7: 66,629,329-66,645,232 , GRCh38.p12 chr7: 67,164,342-67,180,245 TYW1
    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
    nsv442840copy number variation103nstd22human NCBI35 chr2: 179,892,698-179,904,650 , GRCh37.p13 chr2: 180,067,192-180,079,144 , GRCh38.p12 chr2: 179,202,465-179,214,417 SESTD1
    nsv442652copy number variation37nstd22human NCBI35 chr12: 85,203,550-85,215,269 , GRCh37.p13 chr12: 86,701,082-86,712,801 , GRCh38.p12 chr12: 86,307,304-86,319,023 MGAT4C
    nsv442974copy number variation58nstd22human NCBI35 chr1: 111,089,607-111,100,268 , GRCh37.p13 chr1: 111,377,565-111,388,226 , GRCh38.p12 chr1: 110,834,943-110,845,604 NRBF2P3
    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
    nsv442626copy number variation19nstd22human NCBI35 chr11: 104,429,072-104,436,443 , GRCh37.p13 chr11: 104,923,862-104,931,233 , GRCh38.p12 chr11: 105,053,135-105,060,506 LOC107984381
    nsv442965copy number variation36nstd22human NCBI35 chr5: 155,409,350-155,415,307 , GRCh37.p13 chr5: 155,476,772-155,482,729 , GRCh38.p12 chr5: 156,049,762-156,055,719 SGCD
    nsv442666copy number variation87nstd22human NCBI35 chr13: 31,430,622-31,436,423 , GRCh37.p13 chr13: 32,532,622-32,538,423 , GRCh38.p12 chr13: 31,958,485-31,964,286 EEF1DP3
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