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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 RNF103-CHMP3, DAZAP2P1, 2991 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 RNF103-CHMP3, CYP1B1-AS1, 1649 more genes
    nsv3877742copy number variation1nstd102humanPathogenic GRCh37 chr2: 74,365,484-89,129,064 , GRCh38.p12 chr2: 74,138,357-88,829,551 RNF103-CHMP3, RNU6-561P, 253 more genes
    nsv3886532copy number variation1nstd102humanPathogenic GRCh37 chr2: 74,527,522-89,125,488 , GRCh38.p12 chr2: 74,300,395-88,825,975 RNF103-CHMP3, RNU6-561P, 249 more genes
    nsv4451607copy number variation1nstd102humanPathogenic GRCh37 chr2: 77,907,114-87,330,965 , GRCh38.p12 chr2: 77,679,988-87,103,842 RNF103-CHMP3, REEP1, 134 more genes
    nsv6313890copy number variation1nstd102humanPathogenic GRCh37 chr2: 82,486,900-87,322,042 , GRCh38.p12 chr2: 82,259,776-87,094,919 RNF103-CHMP3, LOC105374836, 93 more genes
    nsv3899461copy number variation1nstd102humanPathogenic GRCh38 chr2: 85,014,686-88,826,619 , GRCh37 chr2: 85,241,809-89,126,132 , NCBI36 chr2: 85,095,320-88,907,247 RNF103-CHMP3, CD8A, 115 more genes
    nsv3905336copy number variation1nstd102humanPathogenic NCBI36 chr2: 86,475,806-86,939,918 , GRCh37 chr2: 86,622,295-87,086,407 , GRCh38 chr2: 86,395,172-86,859,284 RNF103-CHMP3, CD8B, 8 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 RNF103-CHMP3, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 RNF103-CHMP3, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 RNF103-CHMP3, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 RNF103-CHMP3, MTND2P22, 3724 more genes
    nsv3916821copy number variation1nstd102humanPathogenic NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722 RNF103-CHMP3, NAGK, 595 more genes
    nsv3897079copy number variation1nstd102humanPathogenic GRCh38 chr2: 77,025,216-90,282,666 , NCBI36 chr2: 77,105,850-90,982,989 , GRCh37 chr2: 77,252,342-91,619,262 RNF103-CHMP3, IGKV2D-18, 280 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 RNF103-CHMP3, ACTG2, 1713 more genes
    nsv3873722copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 86,502,663-87,430,727 , GRCh38.p12 chr2: 86,275,540-87,203,604 RNF103-CHMP3, CD8A, 19 more genes
    nsv3871948copy number variation1nstd102humanBenign GRCh37 chr2: 86,923,178-87,123,114 , GRCh38.p12 chr2: 86,696,055-86,895,991 RNF103-CHMP3, CD8A, 4 more genes
    nsv3903805copy number variation1nstd102humanBenign GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899 RNF103-CHMP3, LOC101927723, 1246 more genes
    nsv3872979copy number variation1nstd102humanBenign GRCh37 chr2: 86,948,478-87,392,543 , GRCh38.p12 chr2: 86,721,355-87,165,420 RNF103-CHMP3, ANAPC1P2, 12 more genes
    nsv6311603copy number variation1nstd102humanUncertain significance GRCh37 chr2: 86,067,267-87,017,948 , GRCh38.p12 chr2: 85,840,144-86,790,825 RNF103-CHMP3, CHMP3-AS1, 16 more genes
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