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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5270826copy number variation1nstd204human GRCh38.p13 chr16: 4,289,501-4,742,300 , GRCh37.p13 chr16: 4,339,502-4,792,301 HMOX2, NMRAL1, 17 more genes
    nsv5008113copy number variation1nstd200human GRCh38 chr16: 4,689,156-4,706,656 , GRCh37.p13 chr16: 4,739,157-4,756,657 MGRN1, NUDT16L1, 1 more genes
    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
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4683689copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,777,699-4,852,592 , GRCh38.p12 chr16: 3,727,698-4,802,591 UBALD1, HMOX2, 30 more genes
    nsv4456218copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,731,117-5,325,699 , GRCh38.p12 chr16: 3,681,116-5,275,698 CORO7-PAM16, DBIP3, 46 more genes
    nsv4453988copy number variation1nstd102humanPathogenic GRCh38 chr16: 3,727,698-4,802,591 , GRCh37 chr16: 3,777,699-4,852,592 RN7SL850P, ZNF500, 30 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4391477copy number variation1nstd171human GRCh37 chr16: 4,737,513-4,737,569 , GRCh38.p12 chr16: 4,687,512-4,687,568 MGRN1, NUDT16L1
    nsv4239355copy number variation1nstd166human GRCh37.p13 chr16: 4,739,978-4,740,323 , GRCh38.p12 chr16: 4,689,977-4,690,322 MGRN1, NUDT16L1
    nsv4238453copy number variation1nstd166human GRCh37.p13 chr16: 4,737,300-4,737,387 , GRCh38.p12 chr16: 4,687,299-4,687,386 NUDT16L1, MGRN1
    nsv4235400copy number variation1nstd166human GRCh37.p13 chr16: 4,712,366-4,795,738 , GRCh38.p12 chr16: 4,662,365-4,745,737 MGRN1, ZNF500, 4 more genes
    nsv3923267copy number variation1nstd102humanPathogenic GRCh37 chr16: 93,732-13,420,663 , GRCh38 chr16: 43,732-13,326,806 , NCBI36 chr16: 33,732-13,328,164 METRN, FAM234A, 413 more genes
    nsv3921068copy number variation1nstd102humanUncertain significance GRCh37 chr16: 4,540,464-4,865,781 , GRCh38 chr16: 4,490,463-4,815,780 , NCBI36 chr16: 4,480,465-4,805,782 SUB1P3, MIR6769A, 14 more genes
    nsv3917929copy number variation1nstd102humanPathogenic GRCh37 chr16: 96,766-11,619,372 , GRCh38 chr16: 46,766-11,525,516 , NCBI36 chr16: 36,766-11,526,873 LOC100130283, PGP, 386 more genes
    nsv3915829copy number variation1nstd102humanPathogenic NCBI36 chr16: 656,663-15,744,462 , GRCh38 chr16: 666,662-15,743,104 , GRCh37 chr16: 716,662-15,836,961 RPL35AP34, LOC100505915, 429 more genes
    nsv3915103copy number variation1nstd102humanPathogenic NCBI36 chr16: 2,972,316-4,981,084 , GRCh37.p13 chr16: 3,032,315-5,041,083 , GRCh38.p12 chr16: 2,982,314-4,991,082 OR1F2P, OR2C1, 101 more genes
    nsv3913858copy number variation1nstd102humanPathogenic GRCh37 chr16: 73,141-11,390,552 , GRCh38 chr16: 23,141-11,296,695 , NCBI36 chr16: 13,141-11,298,053 TPSP1, LUC7L, 382 more genes
    nsv3912877copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,900,735-7,160,698 , NCBI36 chr16: 2,840,736-7,100,699 , GRCh38 chr16: 2,850,734-7,110,697 TRP-CGG1-2, RBFOX1, 129 more genes
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