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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6797207copy number variation1nstd229human GRCh38 chr5: 171,409,854-171,414,038 , GRCh37.p13 chr5: 170,836,858-170,841,042 NPM1
    nsv6795187copy number variation1nstd229human GRCh38 chr5: 171,283,101-171,715,500 , GRCh37.p13 chr5: 170,710,105-171,142,504 RPL19P10, RANBP17, 12 more genes
    nsv6793183copy number variation1nstd229human GRCh38 chr5: 171,394,705-171,399,087 , GRCh37.p13 chr5: 170,821,709-170,826,091 NPM1
    nsv6789317copy number variation1nstd229human GRCh38 chr5: 171,397,686-171,398,021 , GRCh37.p13 chr5: 170,824,690-170,825,025 NPM1
    nsv6787062copy number variation1nstd229human GRCh38 chr5: 171,207,129-171,524,655 , GRCh37.p13 chr5: 170,634,133-170,951,659 RPL10P8, FGF18, 11 more genes
    nsv6786853copy number variation1nstd229human GRCh38 chr5: 171,381,991-171,385,325 , GRCh37.p13 chr5: 170,808,995-170,812,329 MIR3912, NPM1
    nsv6781511copy number variation1nstd229human GRCh38 chr5: 170,662,244-174,111,903 , GRCh37.p13 chr5: 170,089,248-173,538,906 LOC101928093, LOC107986482, 79 more genes
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6289957copy number variation1nstd102humanUncertain significance GRCh37 chr5: 170,814,836-171,100,000 , GRCh38.p12 chr5: 171,387,832-171,672,996 LOC107986392, LOC105377722, 4 more genes
    nsv6136090copy number variation1nstd213human GRCh37 chr5: 161,030,000-172,600,001 , GRCh38.p12 chr5: 161,602,994-173,172,998 BNIP1, CCNG1, 130 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6134988copy number variation1nstd213human GRCh37 chr5: 170,720,000-170,980,001 , GRCh38.p12 chr5: 171,292,996-171,552,997 NPM1, FGF18, 10 more genes
    nsv6018015copy number variation1nstd212human GRCh38 chr5: 171,403,893-171,403,988 , GRCh37.p13 chr5: 170,830,897-170,830,992 NPM1
    nsv6011988copy number variation1nstd212human GRCh38 chr5: 171,403,589-171,403,814 , GRCh37.p13 chr5: 170,830,593-170,830,818 NPM1
    nsv6011730copy number variation1nstd212human GRCh38 chr5: 171,404,170-171,404,254 , GRCh37.p13 chr5: 170,831,174-170,831,258 NPM1
    nsv6006454copy number variation1nstd212human GRCh38 chr5: 171,403,630-171,403,683 , GRCh37.p13 chr5: 170,830,634-170,830,687 NPM1
    nsv6003715copy number variation1nstd212human GRCh38 chr5: 171,403,994-171,404,253 , GRCh37.p13 chr5: 170,830,998-170,831,257 NPM1
    nsv5962419insertion1nstd209human GRCh38 chr5: 171,402,966-171,402,966 , GRCh37.p13 chr5: 170,829,970-170,829,970 NPM1
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