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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
    nsv6796068copy number variation1nstd229human GRCh38 chr5: 171,445,597-171,445,634 , GRCh37.p13 chr5: 170,872,601-170,872,638 FGF18
    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
    nsv6791318copy number variation1nstd229human GRCh38 chr5: 171,443,069-171,443,423 , GRCh37.p13 chr5: 170,870,073-170,870,427 FGF18
    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
    nsv6781750copy number variation1nstd229human GRCh38 chr5: 171,430,506-171,430,813 , GRCh37.p13 chr5: 170,857,510-170,857,817 FGF18
    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
    nsv6781433copy number variation1nstd229human GRCh38 chr5: 171,452,630-171,585,751 , GRCh37.p13 chr5: 170,879,634-171,012,755 FGF18, LOC105377721, 3 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
    nsv6256472mobile element insertion1nstd215human GRCh38 chr5: 171,433,169-171,433,169 , GRCh37.p13 chr5: 170,860,173-170,860,173 FGF18
    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
    nsv5894466copy number variation1nstd209human GRCh38 chr5: 171,415,444-171,420,060 , GRCh37.p13 chr5: 170,842,448-170,847,064 FGF18
    nsv5893155copy number variation1nstd209human GRCh38 chr5: 171,430,493-171,430,812 , GRCh37.p13 chr5: 170,857,497-170,857,816 FGF18
    nsv5569525copy number variation1nstd207human GRCh38 chr5: 171,430,493-171,430,812 , GRCh37.p13 chr5: 170,857,497-170,857,816 FGF18
    nsv5457478copy number variation1nstd206human GRCh38 chr5: 171,421,016-171,421,078 , GRCh37.p13 chr5: 170,848,020-170,848,082 FGF18
    nsv5456682copy number variation1nstd206human GRCh38 chr5: 171,430,506-171,430,813 , GRCh37.p13 chr5: 170,857,510-170,857,817 FGF18
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