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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6810731copy number variation1nstd229human GRCh38 chr6: 149,592,381-149,597,204 , GRCh37.p13 chr6: 149,913,517-149,918,340 RPS18P9, KATNA1
    nsv6799018copy number variation1nstd229human GRCh38 chr6: 149,592,883-149,596,710 , GRCh37.p13 chr6: 149,914,019-149,917,846 RPS18P9, KATNA1
    nsv6617399copy number variation1nstd223human GRCh38 chr6: 149,592,364-149,598,479 , GRCh37.p13 chr6: 149,913,500-149,919,615 RPS18P9, KATNA1
    nsv6571422inversion1nstd223human GRCh38 chr6: 146,996,555-151,115,323 , GRCh37.p13 chr6: 147,317,691-151,436,459 RPSAP40, STXBP5, 62 more genes
    nsv6000921copy number variation1nstd212human GRCh38 chr6: 149,591,033-149,592,374 , GRCh37.p13 chr6: 149,912,169-149,913,510 RPS18P9, GINM1
    nsv5305737copy number variation1nstd204human GRCh37.p13 chr6: 149,912,389-149,913,669 , GRCh38.p13 chr6: 149,591,253-149,592,533 GINM1, RPS18P9
    nsv5238088copy number variation1nstd204human GRCh38.p13 chr6: 149,592,201-149,809,100 , GRCh37.p13 chr6: 149,913,337-150,130,236 , GINM1, 8 more genes
    nsv5235439copy number variation1nstd204human GRCh38.p13 chr6: 149,571,478-149,592,864 , GRCh37.p13 chr6: 149,892,614-149,914,000 GINM1, RPS18P9
    nsv5032313inversion1nstd200human GRCh38 chr6: 149,308,572-149,666,572 , GRCh37.p13 chr6: 149,629,708-149,987,708 TAB2, ZC3H12D, 8 more genes
    nsv4945827copy number variation1nstd200human GRCh38 chr6: 149,592,880-149,596,736 , GRCh37.p13 chr6: 149,914,016-149,917,872 KATNA1, RPS18P9
    nsv4824798copy number variation1nstd200human GRCh37 chr6: 149,914,016-149,917,872 , GRCh38.p12 chr6: 149,592,880-149,596,736 RPS18P9, KATNA1
    nsv4810861copy number variation1nstd200human GRCh37 chr6: 149,913,509-149,918,339 , GRCh38.p12 chr6: 149,592,373-149,597,203 RPS18P9, KATNA1
    nsv4675234copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,431,322-154,120,064 , GRCh38.p12 chr6: 149,110,186-153,798,929 RNU7-3P, HSPD1P16, 86 more genes
    nsv4598749copy number variation1nstd183human GRCh37 chr6: 149,915,949-149,918,515 , GRCh38.p12 chr6: 149,594,813-149,597,379 KATNA1, RPS18P9
    nsv4456488copy number variation1nstd102humanPathogenic GRCh37 chr6: 148,195,086-160,127,254 , GRCh38.p12 chr6: 147,873,950-159,706,222 PDCL3P5, SYTL3, 176 more genes
    nsv4436722copy number variation1nstd102humanPathogenic GRCh37 chr6: 148,690,764-150,494,873 , GRCh38.p12 chr6: 148,369,628-150,173,737 PCMT1, ULBP3, 42 more genes
    nsv4369858copy number variation1nstd173human GRCh37 chr6: 149,892,092-149,941,297 , GRCh38.p12 chr6: 149,570,956-149,620,161 GINM1, KATNA1, 1 more genes
    nsv4369813copy number variation1nstd173human GRCh37 chr6: 149,892,092-149,954,930 , GRCh38.p12 chr6: 149,570,956-149,633,794 GINM1, KATNA1, 1 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4135807copy number variation1nstd166human GRCh37.p13 chr6: 149,905,000-149,931,000 , GRCh38.p12 chr6: 149,583,864-149,609,864 GINM1, RPS18P9, 1 more genes
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