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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123455copy number variation1nstd186human GRCh37 chr16: 82,077,007-82,077,314 , GRCh38.p12 chr16: 82,043,402-82,043,709 HSD17B2, HSD17B2-AS1
    nsv5937722copy number variation1nstd209human GRCh38 chr16: 82,066,430-82,066,487 , GRCh37.p13 chr16: 82,100,035-82,100,092 HSD17B2
    nsv5932402copy number variation1nstd209human GRCh38 chr16: 82,055,483-82,064,585 , GRCh37.p13 chr16: 82,089,088-82,098,190 HSD17B2-AS1, HSD17B2
    nsv5929037copy number variation1nstd209human GRCh38 chr16: 82,043,387-82,043,708 , GRCh37.p13 chr16: 82,076,992-82,077,313 HSD17B2-AS1, HSD17B2
    nsv5884457copy number variation1nstd209human GRCh38 chr16: 82,055,559-82,064,600 , GRCh37.p13 chr16: 82,089,164-82,098,205 HSD17B2, HSD17B2-AS1
    nsv5707812mobile element insertion2nstd211human GRCh38 chr16: 82,055,510-82,055,510 , GRCh37.p13 chr16: 82,089,115-82,089,115 HSD17B2-AS1, HSD17B2
    nsv5585880copy number variation1nstd207human GRCh38 chr16: 82,043,387-82,043,708 , GRCh37.p13 chr16: 82,076,992-82,077,313 HSD17B2, HSD17B2-AS1
    nsv5531243copy number variation1nstd206human GRCh38 chr16: 82,069,175-82,464,363 , GRCh37.p13 chr16: 82,102,780-82,497,968 HSD17B2, MPHOSPH6, 4 more genes
    nsv5528248copy number variation1nstd206human GRCh38 chr16: 82,043,402-82,043,709 , GRCh37.p13 chr16: 82,077,007-82,077,314 HSD17B2-AS1, HSD17B2
    nsv5513972copy number variation1nstd206human GRCh38 chr16: 82,055,491-82,064,586 , GRCh37.p13 chr16: 82,089,096-82,098,191 HSD17B2, HSD17B2-AS1
    nsv5428493mobile element insertion1nstd206human GRCh38 chr16: 82,055,510-82,055,561 , GRCh37.p13 chr16: 82,089,115-82,089,166 HSD17B2, HSD17B2-AS1
    nsv5382945mobile element deletion2nstd186human GRCh37 chr16: 82,077,007-82,077,314 , GRCh38.p12 chr16: 82,043,402-82,043,709 HSD17B2-AS1, HSD17B2
    nsv5358437translocation1nstd200human GRCh38 chr16: 82,040,647-82,040,647 , GRCh38 chr16: 82,040,715-82,040,715 , GRCh37.p13 chr16: 82,074,320-82,074,320 , GRCh37.p13 chr16: 82,074,252-82,074,252 HSD17B2
    nsv5335587translocation1nstd200human GRCh37 chr16: 82,074,320-82,074,320 , GRCh37 chr16: 82,074,252-82,074,252 , GRCh38.p12 chr16: 82,040,647-82,040,647 , GRCh38.p12 chr16: 82,040,715-82,040,715 HSD17B2
    nsv5217811mobile element deletion1nstd204human GRCh37.p13 chr16: 82,077,004-82,077,315 , GRCh38.p13 chr16: 82,043,399-82,043,710 HSD17B2, HSD17B2-AS1
    nsv5158497mobile element insertion1nstd203human GRCh38 chr16: 82,040,532-82,040,548 , GRCh37.p13 chr16: 82,074,137-82,074,153 HSD17B2
    nsv5144699mobile element insertion1nstd203human GRCh38 chr16: 82,056,311-82,056,326 , GRCh37.p13 chr16: 82,089,916-82,089,931 HSD17B2-AS1, HSD17B2
    nsv5013472copy number variation1nstd200human GRCh38 chr16: 82,046,828-82,065,536 , GRCh37.p13 chr16: 82,080,433-82,099,141 HSD17B2-AS1, HSD17B2
    nsv5009717copy number variation1nstd200human GRCh38 chr16: 82,094,625-82,098,673 , GRCh37.p13 chr16: 82,128,230-82,132,278 HSD17B2
    nsv5009716copy number variation1nstd200human GRCh38 chr16: 82,055,491-82,064,586 , GRCh37.p13 chr16: 82,089,096-82,098,191 HSD17B2-AS1, HSD17B2
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