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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094607copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,829,597-11,683,693 , GRCh38.p12 chr16: 8,735,740-11,589,837 LOC400499, NUBP1, 58 more genes
    nsv7076079inversion1nstd229human GRCh38 chr16: 9,015,595-14,846,246 , GRCh37.p13 chr16: 9,109,452-14,940,103 LOC105371093, RNU6-633P, 100 more genes
    nsv6971368copy number variation1nstd229human GRCh38 chr16: 11,255,339-11,255,382 , GRCh37.p13 chr16: 11,349,196-11,349,239 LOC105371082, SOCS1
    nsv6965656copy number variation1nstd229human GRCh38 chr16: 11,235,735-11,254,333 , GRCh37.p13 chr16: 11,329,592-11,348,190 LOC105371082, SOCS1, 1 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6637308copy number variation1nstd102humanUncertain significance GRCh37 chr16: 10,423,631-12,176,517 , GRCh38.p12 chr16: 10,329,774-12,082,660 LOC400499, RSL1D1, 46 more genes
    nsv6507343copy number variation1nstd223human GRCh38 chr16: 10,144,159-11,379,723 , GRCh37.p13 chr16: 10,238,016-11,473,580 LINC01290, LOC105371078, 35 more genes
    nsv6500831copy number variation1nstd223human GRCh38 chr16: 10,669,159-11,475,479 , GRCh37.p13 chr16: 10,763,016-11,569,335 MTCYBP33, MTND4LP24, 27 more genes
    nsv6309886copy number variation2nstd102humanUncertain significance GRCh37 chr16: 8,829,597-11,650,586 , GRCh38.p12 chr16: 8,735,740-11,556,730 NUBP1, TVP23A, 58 more genes
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6133171copy number variation1nstd213human GRCh37 chr16: 10,820,000-11,690,001 , GRCh38.p12 chr16: 10,726,143-11,596,145 CIITA, NUBP1, 21 more genes
    nsv6132975copy number variation1nstd213human GRCh37 chr16: 11,330,000-11,460,001 , GRCh38.p12 chr16: 11,236,143-11,366,144 PRM1, PRM2, 8 more genes
    nsv5381799copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 11,348,700-11,349,387 , GRCh38.p12 chr16: 11,254,843-11,255,530 SOCS1, LOC105371082
    nsv4992715copy number variation1nstd200human GRCh38 chr16: 11,254,995-11,255,228 , GRCh37.p13 chr16: 11,348,852-11,349,085 LOC105371082, SOCS1
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4680676copy number variation1nstd189human GRCh37.p13 chr16: 11,333,398-11,784,674 , GRCh38.p12 chr16: 11,239,541-11,690,818 , PRM1, 15 more genes
    nsv4679254copy number variation1nstd189human GRCh37.p13 chr16: 11,247,365-11,544,021 , GRCh38.p12 chr16: 11,153,508-11,450,165 PRM1, PRM2, 12 more genes
    nsv4678852copy number variation1nstd189human GRCh37.p13 chr16: 11,303,331-11,581,403 , GRCh38.p12 chr16: 11,209,474-11,487,547 PRM1, PRM2, 12 more genes
    nsv4627808copy number variation1nstd183human GRCh37 chr16: 11,348,209-11,349,009 , GRCh38.p12 chr16: 11,254,352-11,255,152 LOC105371082, SOCS1
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