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Items: 1 to 20 of 267

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964543insertion1nstd209human GRCh38 chr3: 9,445,964-9,445,964 , GRCh37.p13 chr3: 9,487,648-9,487,648 SETD5
    nsv5897442copy number variation1nstd209human GRCh38 chr3: 9,457,214-9,459,495 , GRCh37.p13 chr3: 9,498,898-9,501,179 SETD5
    nsv5837465copy number variation1nstd209human GRCh38 chr3: 9,457,886-9,459,585 , GRCh37.p13 chr3: 9,499,570-9,501,269 SETD5
    nsv5678567mobile element insertion2nstd211human GRCh38 chr3: 9,445,988-9,445,988 , GRCh37.p13 chr3: 9,487,672-9,487,672 SETD5
    nsv5557885sequence alteration1nstd206human GRCh37.p13 chr3: 9,254,033-9,464,050 , GRCh38 chr3: 9,212,349-9,422,366 SRGAP3, THUMPD3, 5 more genes
    nsv5448817copy number variation1nstd206human GRCh38 chr3: 9,412,587-9,417,483 , GRCh37.p13 chr3: 9,454,271-9,459,167 SETD5
    nsv5444253copy number variation1nstd206human GRCh38 chr3: 9,421,817-9,422,063 , GRCh37.p13 chr3: 9,463,501-9,463,747 SETD5
    nsv5351431translocation1nstd200human GRCh38 chr3: 9,412,175-9,412,175 , GRCh38 chr3: 9,410,480-9,410,480 , GRCh37.p13 chr3: 9,452,164-9,452,164 , GRCh37.p13 chr3: 9,453,859-9,453,859 SETD5
    nsv5345893translocation1nstd200human GRCh37 chr3: 9,453,859-9,453,859 , GRCh37 chr3: 9,452,164-9,452,164 , GRCh38.p12 chr3: 9,412,175-9,412,175 , GRCh38.p12 chr3: 9,410,480-9,410,480 SETD5
    nsv5309727copy number variation1nstd204human GRCh38.p13 chr3: 9,412,578-9,417,512 , GRCh37.p13 chr3: 9,454,262-9,459,196 SETD5
    nsv5307148copy number variation1nstd204human GRCh38.p13 chr3: 9,409,811-9,413,262 , GRCh37.p13 chr3: 9,451,495-9,454,946 SETD5
    nsv5219320copy number variation1nstd204human GRCh38.p13 chr3: 9,417,501-9,422,400 , GRCh37.p13 chr3: 9,459,185-9,464,084 SETD5
    nsv5219209copy number variation1nstd204human GRCh38.p13 chr3: 9,409,561-9,413,146 , GRCh37.p13 chr3: 9,451,245-9,454,830 SETD5
    nsv5211399copy number variation1nstd204human GRCh38.p13 chr3: 9,419,136-9,422,430 , GRCh37.p13 chr3: 9,460,820-9,464,114 SETD5
    nsv5203333copy number variation1nstd204human GRCh38.p13 chr3: 9,412,422-9,417,575 , GRCh37.p13 chr3: 9,454,106-9,459,259 SETD5
    nsv5075163mobile element insertion1nstd203human GRCh38 chr3: 9,426,213-9,426,252 , GRCh37.p13 chr3: 9,467,897-9,467,936 SETD5
    nsv5071914mobile element insertion1nstd203human GRCh38 chr3: 9,462,996-9,463,013 , GRCh37.p13 chr3: 9,504,680-9,504,697 SETD5
    nsv5068860mobile element insertion1nstd203human GRCh38 chr3: 9,426,216-9,426,252 , GRCh37.p13 chr3: 9,467,900-9,467,936 SETD5
    nsv5066157mobile element insertion1nstd203human GRCh38 chr3: 9,432,121-9,432,138 , GRCh37.p13 chr3: 9,473,805-9,473,822 SETD5
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
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