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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980449copy number variation1nstd102humanrisk factor GRCh37 chr3: 195,693,872-197,376,871 , GRCh38.p12 chr3: 195,967,001-197,650,000 RN7SL434P, RNU6-1279P, 54 more genes
    nsv5975867inversion1nstd209human GRCh38 chr3: 196,245,165-196,619,601 , GRCh37.p13 chr3: 195,972,036-196,346,472 PCYT1A, UBXN7, 17 more genes
    nsv5948636insertion1nstd209human GRCh38 chr3: 196,289,898-196,289,898 , GRCh37.p13 chr3: 196,016,769-196,016,769 DYNLT2B
    nsv5835803copy number variation1nstd209human GRCh38 chr3: 196,308,087-196,309,786 , GRCh37.p13 chr3: 196,034,958-196,036,657 DYNLT2B
    nsv5730788mobile element insertion1nstd211human GRCh38 chr3: 196,290,452-196,290,452 , GRCh37.p13 chr3: 196,017,323-196,017,323 DYNLT2B
    nsv5619188insertion1nstd207human GRCh38 chr3: 196,317,476-196,317,476 , GRCh37.p13 chr3: 196,044,347-196,044,347 DYNLT2B, TM4SF19-DYNLT2B, 2 more genes
    nsv5616996insertion1nstd207human GRCh38 chr3: 196,317,484-196,317,484 , GRCh37.p13 chr3: 196,044,355-196,044,355 DYNLT2B, TM4SF19-DYNLT2B, 2 more genes
    nsv5608010insertion1nstd207human GRCh38 chr3: 196,317,377-196,317,377 , GRCh37.p13 chr3: 196,044,248-196,044,248 DYNLT2B, TM4SF19-DYNLT2B, 2 more genes
    nsv5573320copy number variation1nstd207human GRCh38 chr3: 196,317,394-196,317,477 , GRCh37.p13 chr3: 196,044,265-196,044,348 DYNLT2B, TM4SF19-DYNLT2B, 2 more genes
    nsv5563557sequence alteration1nstd206human GRCh38 chr3: 196,244,777-196,619,867 , GRCh37.p13 chr3: 195,971,648-196,346,738 PCYT1A, FBXO45, 17 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5452734copy number variation1nstd206human GRCh38 chr3: 196,295,030-196,299,308 , GRCh37.p13 chr3: 196,021,901-196,026,179 DYNLT2B
    nsv5441418copy number variation1nstd206human GRCh38 chr3: 196,317,090-196,317,470 , GRCh37.p13 chr3: 196,043,961-196,044,341 DYNLT2B, LOC107986031, 2 more genes
    nsv5434383copy number variation1nstd206human GRCh38 chr3: 196,305,692-196,306,359 , GRCh37.p13 chr3: 196,032,563-196,033,230 DYNLT2B
    nsv5381417copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,754,030-196,438,852 , GRCh38.p12 chr3: 196,027,159-196,711,981 PIGX, TM4SF19-DYNLT2B, 28 more genes
    nsv5237696copy number variation1nstd204human GRCh38.p13 chr3: 196,295,401-196,501,800 , GRCh37.p13 chr3: 196,022,272-196,228,671 TM4SF19, UBXN7, 11 more genes
    nsv5200370copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,419,168-197,387,258 , GRCh38.p12 chr3: 195,692,297-197,660,387 NCBP2AS2, DLG1-AS1, 67 more genes
    nsv5200362copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,747,856-197,387,258 , GRCh38.p12 chr3: 196,020,985-197,660,387 MIR4797, SDHAP4, 52 more genes
    nsv4928444copy number variation1nstd200human GRCh38 chr3: 196,318,722-196,320,049 , GRCh37.p13 chr3: 196,045,593-196,046,920 TM4SF19-DYNLT2B, TM4SF19-AS1, 1 more genes
    nsv4928443copy number variation1nstd200human GRCh38 chr3: 196,305,720-196,306,309 , GRCh37.p13 chr3: 196,032,591-196,033,180 DYNLT2B
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