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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977749insertion1nstd209human GRCh38 chr15: 88,897,561-88,897,561 , GRCh37.p13 chr15: 89,440,792-89,440,792 MFGE8
    nsv5944658copy number variation1nstd209human GRCh38 chr15: 88,897,512-88,897,563 , GRCh37.p13 chr15: 89,440,743-89,440,794 MFGE8
    nsv5940726copy number variation1nstd209human GRCh38 chr15: 88,901,183-88,901,244 , GRCh37.p13 chr15: 89,444,414-89,444,475 MFGE8
    nsv5660417insertion2nstd207human GRCh38 chr15: 88,897,514-88,897,514 , GRCh37.p13 chr15: 89,440,745-89,440,745 MFGE8
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5009149copy number variation1nstd200human GRCh38 chr15: 88,891,164-89,121,215 , GRCh37.p13 chr15: 89,434,395-89,664,446 ABHD2, MFGE8, 5 more genes
    nsv5009147copy number variation1nstd200human GRCh38 chr15: 88,678,823-88,931,767 , GRCh37.p13 chr15: 89,222,054-89,474,998 MFGE8, HAPLN3, 2 more genes
    nsv5002265copy number variation1nstd200human GRCh38 chr15: 88,911,023-88,911,114 , GRCh37.p13 chr15: 89,454,254-89,454,345 MFGE8
    nsv4863945copy number variation1nstd200human GRCh37 chr15: 89,222,054-89,474,998 , GRCh38.p12 chr15: 88,678,823-88,931,767 MFGE8, LOC105370960, 2 more genes
    nsv4730855copy number variation1nstd199human GRCh37 chr15: 89,444,235-89,444,364 , GRCh38.p12 chr15: 88,901,004-88,901,133 MFGE8
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4725974insertion1nstd186human GRCh37 chr15: 89,440,745-89,440,745 , GRCh38.p12 chr15: 88,897,514-88,897,514 MFGE8
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4673073copy number variation1nstd186human GRCh37 chr15: 89,456,419-89,544,859 , GRCh38.p12 chr15: 88,913,188-89,001,628 MFGE8, KRT18P47, 1 more genes
    nsv4629797copy number variation1nstd183human GRCh37 chr15: 89,445,598-89,468,913 , GRCh38.p12 chr15: 88,902,367-88,925,682 MFGE8
    nsv4627093copy number variation2nstd183human GRCh37 chr15: 89,456,419-89,544,859 , GRCh38.p12 chr15: 88,913,188-89,001,628 MFGE8, LOC100129942, 1 more genes
    nsv4539875insertion1nstd166human GRCh37.p13 chr15: 89,440,745-89,440,745 , GRCh38.p12 chr15: 88,897,514-88,897,514 MFGE8
    nsv4447104insertion1nstd175human GRCh37 chr15: 89,440,745-89,440,745 , GRCh38.p12 chr15: 88,897,514-88,897,514 MFGE8
    nsv4377776copy number variation1nstd173human GRCh37 chr15: 86,980,083-93,499,239 , GRCh38.p12 chr15: 86,436,852-92,956,009 , RNU6-1111P, 136 more genes
    nsv4350274copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,883,823-92,165,844 , GRCh38.p12 chr15: 83,215,071-91,622,614 AKAP13, LOC105370972, 184 more genes
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