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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095031copy number variation2nstd102humanPathogenic GRCh37 chr16: 56,226,148-58,768,132 , GRCh38.p12 chr16: 56,192,236-58,734,228 MT1B, LOC105371293, 92 more genes
    nsv7094589copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,016,057-58,768,132 , GRCh38.p12 chr16: 56,982,145-58,734,228 SLC38A7, SETD6, 58 more genes
    nsv7073134inversion1nstd229human GRCh38 chr16: 58,500,288-58,500,361 , GRCh37.p13 chr16: 58,534,192-58,534,265 NDRG4
    nsv7069876inversion1nstd229human GRCh38 chr16: 58,076,774-64,694,512 , GRCh37.p13 chr16: 58,110,678-64,728,415 RN7SKP76, LOC105371311, 57 more genes
    nsv7069696inversion1nstd229human GRCh38 chr16: 58,205,688-64,165,972 , GRCh37.p13 chr16: 58,239,592-64,199,876 GOT2, RNU6-103P, 49 more genes
    nsv6991770copy number variation1nstd229human GRCh38 chr16: 58,495,319-58,498,882 , GRCh37.p13 chr16: 58,529,223-58,532,786 NDRG4, RNU6-103P
    nsv6990550copy number variation1nstd229human GRCh38 chr16: 58,499,401-58,502,300 , GRCh37.p13 chr16: 58,533,305-58,536,204 NDRG4
    nsv6987321copy number variation1nstd229human GRCh38 chr16: 58,399,861-58,468,278 , GRCh37.p13 chr16: 58,433,765-58,502,182 NDRG4, LINC02137, 1 more genes
    nsv6986392copy number variation1nstd229human GRCh38 chr16: 58,472,172-58,475,844 , GRCh37.p13 chr16: 58,506,076-58,509,748 NDRG4
    nsv6985159copy number variation1nstd229human GRCh38 chr16: 58,468,694-58,471,701 , GRCh37.p13 chr16: 58,502,598-58,505,605 NDRG4
    nsv6978953copy number variation1nstd229human GRCh38 chr16: 58,509,352-58,511,421 , GRCh37.p13 chr16: 58,543,256-58,545,325 NDRG4
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6511280copy number variation1nstd223human GRCh38 chr16: 58,489,107-58,490,998 , GRCh37.p13 chr16: 58,523,011-58,524,902 NDRG4
    nsv6510575copy number variation1nstd223human GRCh38 chr16: 58,468,694-58,471,696 , GRCh37.p13 chr16: 58,502,598-58,505,600 NDRG4
    nsv6502718copy number variation1nstd223human GRCh38 chr16: 58,489,052-58,490,996 , GRCh37.p13 chr16: 58,522,956-58,524,900 NDRG4
    nsv6499119copy number variation1nstd223human GRCh38 chr16: 58,484,701-58,486,400 , GRCh37.p13 chr16: 58,518,605-58,520,304 NDRG4
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5930825copy number variation1nstd209human GRCh38 chr16: 58,489,033-58,491,066 , GRCh37.p13 chr16: 58,522,937-58,524,970 NDRG4
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