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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7057573inversion1nstd229human GRCh38 chr2: 207,521,365-209,493,860 , GRCh37.p13 chr2: 208,386,089-210,358,584 CRYGEP, CRYGFP, 40 more genes
    nsv6682898copy number variation1nstd229human GRCh38 chr2: 207,759,496-207,777,884 , GRCh37.p13 chr2: 208,624,220-208,642,608 FZD5
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 LOC100421409, LOC100507443, 310 more genes
    nsv6315398copy number variation1nstd102humanPathogenic GRCh37 chr2: 185,697,659-213,002,074 , GRCh38.p12 chr2: 184,832,932-212,137,349 LOC107985785, MYO1B, 381 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313730copy number variation1nstd102humanPathogenic GRCh37 chr2: 200,851,079-209,054,267 , GRCh38.p12 chr2: 199,986,356-208,189,543 RN7SKP200, PIMREGP1, 179 more genes
    nsv6311631copy number variation1nstd102humanUncertain significance GRCh37 chr2: 203,420,070-211,811,277 , GRCh38.p12 chr2: 202,555,347-210,946,553 MIR3130-2, WDR12, 133 more genes
    nsv6292094mobile element insertion1nstd186human GRCh37 chr2: 208,620,695-208,620,746 , GRCh38.p12 chr2: 207,755,971-207,756,022 FZD5, CCNYL1
    nsv5684289mobile element insertion2nstd211human GRCh38 chr2: 207,755,971-207,755,971 , GRCh37.p13 chr2: 208,620,695-208,620,695 FZD5, CCNYL1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5412535mobile element insertion1nstd206human GRCh38 chr2: 207,755,971-207,756,022 , GRCh37.p13 chr2: 208,620,695-208,620,746 FZD5, CCNYL1
    nsv5318715copy number variation1nstd204human GRCh38.p13 chr2: 207,759,076-207,765,612 , GRCh37.p13 chr2: 208,623,800-208,630,336 FZD5
    nsv5217052copy number variation1nstd204human GRCh38.p13 chr2: 207,759,059-207,765,540 , GRCh37.p13 chr2: 208,623,783-208,630,264 FZD5
    nsv5079578mobile element insertion1nstd203human GRCh38 chr2: 207,757,825-207,757,839 , GRCh37.p13 chr2: 208,622,549-208,622,563 FZD5
    nsv5070014mobile element insertion1nstd203human GRCh38 chr2: 207,757,276-207,757,289 , GRCh37.p13 chr2: 208,622,000-208,622,013 FZD5
    nsv5063504mobile element insertion1nstd203human GRCh38 chr2: 207,755,954-207,755,971 , GRCh37.p13 chr2: 208,620,678-208,620,695 CCNYL1, FZD5
    nsv5033412inversion1nstd200human GRCh38 chr2: 206,107,842-207,979,103 , GRCh37.p13 chr2: 206,972,566-208,843,827 ATP5POP1, MIR2355, 39 more genes
    nsv4916513copy number variation1nstd200human GRCh38 chr2: 207,759,081-207,765,609 , GRCh37.p13 chr2: 208,623,805-208,630,333 FZD5
    nsv4913874copy number variation1nstd200human GRCh38 chr2: 207,765,014-207,765,210 , GRCh37.p13 chr2: 208,629,738-208,629,934 FZD5
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