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Items: 1 to 20 of 334

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148264copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,658,260-25,114,888 , GRCh38.p12 chr22: 23,316,073-24,718,921 LOC100421614, ZNF70, 60 more genes
    nsv7075178inversion1nstd229human GRCh38 chr22: 24,760,969-24,761,006 , GRCh37.p13 chr22: 25,156,936-25,156,973 PIWIL3
    nsv7073239inversion1nstd229human GRCh38 chr22: 24,707,166-24,833,990 , GRCh37.p13 chr22: 25,103,133-25,229,957 TOP1P2, PIWIL3, 3 more genes
    nsv7073094inversion1nstd229human GRCh38 chr22: 22,618,607-30,089,219 , GRCh37.p13 chr22: 22,961,077-30,485,208 BCRP1, POM121L10P, 237 more genes
    nsv7072924inversion1nstd229human GRCh38 chr22: 23,614,290-25,377,289 , GRCh37.p13 chr22: 23,956,477-25,773,256 DDTL, SUSD2, 58 more genes
    nsv7071742inversion1nstd229human GRCh38 chr22: 23,575,130-25,318,153 , GRCh37.p13 chr22: 23,917,317-25,714,120 UPB1, LOC107985577, 57 more genes
    nsv7067842inversion1nstd229human GRCh38 chr22: 23,575,725-25,317,505 , GRCh37.p13 chr22: 23,917,912-25,713,472 CHCHD10, ZNF70, 57 more genes
    nsv7067453inversion1nstd229human GRCh38 chr22: 23,866,674-25,883,003 , GRCh37.p13 chr22: 24,208,861-26,278,970 CRIP1P4, LOC100129358, 54 more genes
    nsv7067351inversion1nstd229human GRCh38 chr22: 24,412,391-26,256,987 , GRCh37.p13 chr22: 24,808,359-26,652,953 BCRP3, GGT1, 40 more genes
    nsv7067181inversion1nstd229human GRCh38 chr22: 24,773,597-24,773,641 , GRCh37.p13 chr22: 25,169,564-25,169,608 PIWIL3
    nsv7063732inversion1nstd229human GRCh38 chr22: 23,598,898-25,431,054 , GRCh37.p13 chr22: 23,941,085-25,827,021 LOC100652871, CRYBB2, 58 more genes
    nsv7062268inversion1nstd229human GRCh38 chr22: 23,594,836-25,435,234 , GRCh37.p13 chr22: 23,937,023-25,831,201 KIAA1671-AS1, BCRP3, 58 more genes
    nsv7061931inversion1nstd229human GRCh38 chr22: 24,713,125-24,717,189 , GRCh37.p13 chr22: 25,109,092-25,113,156 CRIP1P4, PIWIL3
    nsv7034499copy number variation1nstd229human GRCh38 chr22: 24,736,367-24,750,884 , GRCh37.p13 chr22: 25,132,334-25,146,851 PIWIL3
    nsv7033057copy number variation1nstd229human GRCh38 chr22: 24,735,265-24,735,531 , GRCh37.p13 chr22: 25,131,232-25,131,498 PIWIL3
    nsv7032395copy number variation1nstd229human GRCh38 chr22: 24,728,836-24,739,869 , GRCh37.p13 chr22: 25,124,803-25,135,836 PIWIL3
    nsv7029830copy number variation1nstd229human GRCh38 chr22: 24,393,949-25,090,115 , GRCh37.p13 chr22: 24,789,917-25,486,082 SGSM1, LOC100421614, 19 more genes
    nsv7029762copy number variation1nstd229human GRCh38 chr22: 24,773,986-24,836,949 , GRCh37.p13 chr22: 25,169,953-25,232,916 SGSM1, PIWIL3
    nsv7028873copy number variation1nstd229human GRCh38 chr22: 22,977,123-28,064,565 , GRCh37.p13 chr22: 23,319,297-28,460,553 LOC100652871, VPREB3, 132 more genes
    nsv7028011copy number variation1nstd229human GRCh38 chr22: 24,730,930-24,741,124 , GRCh37.p13 chr22: 25,126,897-25,137,091 PIWIL3
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