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Items: 1 to 20 of 395

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906374copy number variation1nstd209human GRCh38 chr2: 158,128,799-158,129,679 , GRCh37.p13 chr2: 158,985,311-158,986,191 UPP2
    nsv5903502copy number variation1nstd209human GRCh38 chr2: 158,033,958-158,034,088 , GRCh37.p13 chr2: 158,890,470-158,890,600 UPP2
    nsv5894836copy number variation1nstd209human GRCh38 chr2: 158,116,851-158,122,747 , GRCh37.p13 chr2: 158,973,363-158,979,259 UPP2
    nsv5831968copy number variation1nstd209human GRCh38 chr2: 158,116,843-158,122,642 , GRCh37.p13 chr2: 158,973,355-158,979,154 UPP2
    nsv5727831mobile element insertion2nstd211human GRCh38 chr2: 158,106,680-158,106,680 , GRCh37.p13 chr2: 158,963,192-158,963,192 UPP2
    nsv5688394mobile element insertion1nstd211human GRCh38 chr2: 158,066,546-158,066,546 , GRCh37.p13 chr2: 158,923,058-158,923,058 UPP2, PTP4A1P1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5557732mobile element insertion1nstd206human GRCh38 chr2: 158,106,692-158,106,731 , GRCh37.p13 chr2: 158,963,204-158,963,243 UPP2
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5452336copy number variation1nstd206human GRCh38 chr2: 158,116,853-158,122,748 , GRCh37.p13 chr2: 158,973,365-158,979,260 UPP2
    nsv5446912copy number variation1nstd206human GRCh38 chr2: 158,033,958-158,034,089 , GRCh37.p13 chr2: 158,890,470-158,890,601 UPP2
    nsv5446199copy number variation1nstd206human GRCh38 chr2: 158,128,799-158,129,697 , GRCh37.p13 chr2: 158,985,311-158,986,209 UPP2
    nsv5444081copy number variation1nstd206human GRCh38 chr2: 157,994,589-157,994,660 , GRCh37.p13 chr2: 158,851,101-158,851,172 UPP2
    nsv5439010copy number variation1nstd206human GRCh38 chr2: 158,007,083-158,007,195 , GRCh37.p13 chr2: 158,863,595-158,863,707 UPP2
    nsv5435581copy number variation1nstd206human GRCh38 chr2: 158,098,602-158,104,017 , GRCh37.p13 chr2: 158,955,114-158,960,529 UPP2
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5412726mobile element insertion1nstd206human GRCh38 chr2: 158,066,546-158,066,556 , GRCh37.p13 chr2: 158,923,058-158,923,068 UPP2, PTP4A1P1
    nsv5350902translocation1nstd200human GRCh38 chr2: 158,128,799-158,128,799 , GRCh38 chr2: 158,129,697-158,129,697 , GRCh37.p13 chr2: 158,985,311-158,985,311 , GRCh37.p13 chr2: 158,986,209-158,986,209 UPP2
    nsv5345406translocation1nstd200human GRCh37 chr2: 158,986,209-158,986,209 , GRCh37 chr2: 158,985,311-158,985,311 , GRCh38.p12 chr2: 158,129,697-158,129,697 , GRCh38.p12 chr2: 158,128,799-158,128,799 UPP2
    nsv5327227inversion1nstd204human GRCh37.p13 chr2: 151,300,232-168,612,803 , GRCh38.p13 chr2: 150,443,718-167,756,293 , RND3, 198 more genes
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