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Items: 1 to 20 of 39

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4387453copy number variation1nstd173human GRCh37 chrX: 154,875,920-154,953,109 , GRCh38.p12 chrX: 155,646,259-155,723,447 SPRY3
    nsv4372152copy number variation236nstd173human GRCh37 chr6: 78,969,092-79,035,184 , GRCh38.p12 chr6: 78,259,375-78,325,467 LOC105377865
    nsv4365227copy number variation7nstd173human GRCh37 chr11: 49,703,510-49,758,260 , GRCh38.p12 chr11: 49,681,958-49,736,708 , GRCh38.p12 chr11|NW_019805495.1: 146,138-200,857 GRM5P1
    nsv4371997copy number variation1nstd173human GRCh37 chr2: 98,855,690-98,891,096 , GRCh38.p12 chr2: 98,239,227-98,274,633 VWA3B
    nsv4365926copy number variation7nstd173human GRCh37 chr20: 1,560,549-1,593,892 , GRCh38.p12 chr20: 1,579,903-1,613,246 SIRPB1
    nsv4372073copy number variation11nstd173human GRCh37 chr16: 20,512,753-20,545,824 , GRCh38.p12 chr16: 20,501,431-20,534,502 ACSM2B
    nsv4367758copy number variation1nstd173human GRCh37 chr6: 78,880,820-78,911,021 , GRCh38.p12 chr6: 78,171,103-78,201,304 LOC105377865
    nsv4384438copy number variation5nstd173human GRCh37 chr11: 21,183,993-21,212,091 , GRCh38.p12 chr11: 21,162,447-21,190,545 NELL1
    nsv4373812copy number variation14nstd173human GRCh37 chr11: 7,809,465-7,837,000 , GRCh38.p12 chr11: 7,787,918-7,815,453 , GRCh38.p12 chr11|NT_187583.1: 8,786-36,321 , GRCh38.p12 chr11|NW_011332695.1: 8,786-36,332 OR5P2
    nsv4368630copy number variation19nstd173human GRCh37 chr13: 57,750,941-57,778,379 , GRCh38.p12 chr13: 57,176,807-57,204,245 MTCO2P3
    nsv4386489copy number variation3nstd173human GRCh37 chr8: 75,308,305-75,331,619 , GRCh38.p12 chr8: 74,396,070-74,419,384 GDAP1
    nsv4378281copy number variation14nstd173human GRCh37 chr13: 69,248,299-69,269,380 , GRCh38.p12 chr13: 68,674,167-68,695,248 RN7SL761P
    nsv4369986copy number variation2nstd173human GRCh37 chr2: 55,908,926-55,938,566 , GRCh38.p12 chr2: 55,681,791-55,711,431 PNPT1
    nsv4370116copy number variation174nstd173human GRCh37 chr2: 98,138,417-98,161,960 , GRCh38.p12 chr2: 97,521,954-97,545,497 ANKRD36B
    nsv4366472copy number variation183nstd173human GRCh37 chr3: 46,793,072-46,849,588 , GRCh38.p12 chr3: 46,751,582-46,808,098 PRSS44P, PRSS43P
    nsv4370405copy number variation14nstd173human GRCh37 chr12: 11,503,224-11,553,849 , GRCh38.p12 chr12: 11,350,290-11,400,915 , GRCh38.p12 chr12|NT_187658.1: 545,253-572,349 PRB1, PRB2
    nsv4382019copy number variation1nstd173human GRCh37 chrX: 150,673,093-150,722,241 , GRCh38.p12 chrX: 151,504,621-151,553,769 LOC105373367, LOC105377213
    nsv4373620copy number variation1nstd173human GRCh37 chr1: 196,828,725-196,877,049 , GRCh38.p12 chr1: 196,859,595-196,907,919 CFHR4, LOC100996886
    nsv4385056copy number variation1nstd173human GRCh37 chr15: 31,352,074-31,392,865 , GRCh38.p12 chr15: 31,059,871-31,100,662 , GRCh38.p12 chr15|NT_187660.1: 3,345,629-3,386,398 , GRCh38.p12 chr15|NW_011332701.1: 3,233,177-3,273,946 TRPM1, MIR211
    nsv4380983copy number variation1nstd173human GRCh37 chr5: 115,543,432-115,575,190 , GRCh38.p12 chr5: 116,207,735-116,239,493 HMGN2P27, COMMD10
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