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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962419insertion1nstd209human GRCh38 chr5: 171,402,966-171,402,966 , GRCh37.p13 chr5: 170,829,970-170,829,970 NPM1
    nsv5576854copy number variation1nstd207human GRCh38 chr5: 171,403,994-171,404,252 , GRCh37.p13 chr5: 170,830,998-170,831,256 NPM1
    nsv5539330insertion1nstd206human GRCh38 chr5: 171,398,098-171,398,136 , GRCh37.p13 chr5: 170,825,102-170,825,140 NPM1
    nsv5464265copy number variation1nstd206human GRCh38 chr5: 171,397,686-171,398,021 , GRCh37.p13 chr5: 170,824,690-170,825,025 NPM1
    nsv5238766copy number variation1nstd204human GRCh38.p13 chr5: 171,403,801-171,404,400 , GRCh37.p13 chr5: 170,830,805-170,831,404 NPM1
    nsv5090943mobile element insertion1nstd203human GRCh38 chr5: 171,398,085-171,398,098 , GRCh37.p13 chr5: 170,825,089-170,825,102 NPM1
    nsv4949219copy number variation1nstd200human GRCh38 chr5: 171,346,066-171,385,894 , GRCh37.p13 chr5: 170,773,070-170,812,898 RPL10P8, RN7SL339P, 5 more genes
    nsv4939896copy number variation1nstd200human GRCh38 chr5: 171,396,249-171,398,074 , GRCh37.p13 chr5: 170,823,253-170,825,078 NPM1
    nsv4939895copy number variation1nstd200human GRCh38 chr5: 171,395,995-171,398,131 , GRCh37.p13 chr5: 170,822,999-170,825,135 NPM1
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4763538inversion1nstd199human GRCh37 chr5: 170,260,689-178,183,120 , GRCh38.p12 chr5: 170,833,685-178,756,119 , BNIP1, 194 more genes
    nsv4750050copy number variation1nstd199human GRCh37 chr5: 170,830,885-170,831,117 , GRCh38.p12 chr5: 171,403,881-171,404,113 NPM1
    nsv4578263copy number variation1nstd102humanPathogenic GRCh37 chr5: 166,420,934-173,324,844 , GRCh38.p12 chr5: 166,993,929-173,897,841 LINC01187, TENM2-AS1, 112 more genes
    nsv4542095insertion1nstd166human GRCh37.p13 chr5: 170,825,089-170,825,089 , GRCh38.p12 chr5: 171,398,085-171,398,085 NPM1
    nsv4455586copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,597,181-171,166,353 , GRCh38.p12 chr5: 157,170,170-171,739,349 LOC105377677, GABRA6, 164 more genes
    nsv4443363copy number variation1nstd175human GRCh37 chr5: 170,830,529-170,830,755 , GRCh38.p12 chr5: 171,403,525-171,403,751 NPM1
    nsv4128441copy number variation1nstd166human GRCh37.p13 chr5: 170,531,533-171,085,237 , GRCh38.p12 chr5: 171,104,529-171,658,233 LOC107986392, RN7SL339P, 13 more genes
    nsv4120680copy number variation1nstd166human GRCh37.p13 chr5: 170,634,133-170,951,659 , GRCh38.p12 chr5: 171,207,129-171,524,655 RN7SL339P, TLX3, 11 more genes
    nsv4120185copy number variation1nstd166human GRCh37.p13 chr5: 170,773,070-170,812,898 , GRCh38.p12 chr5: 171,346,066-171,385,894 NPM1, RPL10P8, 5 more genes
    nsv4117961copy number variation1nstd166human GRCh37.p13 chr5: 170,835,658-170,837,486 , GRCh38.p12 chr5: 171,408,654-171,410,482 NPM1
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