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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973557insertion1nstd209human GRCh38 chr14: 52,623,233-52,623,233 , GRCh37.p13 chr14: 53,089,951-53,089,951 GPR137C
    nsv5942631copy number variation1nstd209human GRCh38 chr14: 52,559,510-52,564,933 , GRCh37.p13 chr14: 53,026,228-53,031,651 GPR137C
    nsv5940593copy number variation1nstd209human GRCh38 chr14: 52,576,969-52,587,340 , GRCh37.p13 chr14: 53,043,687-53,054,058 GPR137C
    nsv5939496copy number variation1nstd209human GRCh38 chr14: 52,573,398-52,591,494 , GRCh37.p13 chr14: 53,040,116-53,058,212 GPR137C
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5867169copy number variation1nstd209human GRCh38 chr14: 52,559,542-52,564,941 , GRCh37.p13 chr14: 53,026,260-53,031,659 GPR137C
    nsv5861057copy number variation1nstd209human GRCh38 chr14: 52,575,537-52,587,791 , GRCh37.p13 chr14: 53,042,255-53,054,509 GPR137C
    nsv5849372copy number variation1nstd209human GRCh38 chr14: 52,573,396-52,576,986 , GRCh37.p13 chr14: 53,040,114-53,043,704 GPR137C
    nsv5848078copy number variation1nstd209human GRCh38 chr14: 52,589,898-52,591,906 , GRCh37.p13 chr14: 53,056,616-53,058,624 GPR137C
    nsv5728600mobile element insertion1nstd211human GRCh38 chr14: 52,637,967-52,637,967 , GRCh37.p13 chr14: 53,104,685-53,104,685 GPR137C, ERO1A
    nsv5720283mobile element insertion1nstd211human GRCh38 chr14: 52,565,734-52,565,734 , GRCh37.p13 chr14: 53,032,452-53,032,452 GPR137C
    nsv5699999mobile element insertion2nstd211human GRCh38 chr14: 52,623,243-52,623,243 , GRCh37.p13 chr14: 53,089,961-53,089,961 GPR137C
    nsv5548918insertion1nstd206human GRCh38 chr14: 52,637,967-52,638,004 , GRCh37.p13 chr14: 53,104,685-53,104,722 GPR137C, ERO1A
    nsv5510536copy number variation1nstd206human GRCh38 chr14: 52,573,392-52,573,444 , GRCh37.p13 chr14: 53,040,110-53,040,162 GPR137C
    nsv5494651copy number variation1nstd206human GRCh38 chr14: 52,559,510-52,564,934 , GRCh37.p13 chr14: 53,026,228-53,031,652 GPR137C
    nsv5428874mobile element insertion1nstd206human GRCh38 chr14: 52,623,243-52,623,294 , GRCh37.p13 chr14: 53,089,961-53,090,012 GPR137C
    nsv5357254translocation1nstd200human GRCh38 chr14: 52,610,262-52,610,262 , GRCh38 chr14: 52,610,329-52,610,329 , GRCh37.p13 chr14: 53,076,980-53,076,980 , GRCh37.p13 chr14: 53,077,047-53,077,047 GPR137C
    nsv5357253translocation1nstd200human GRCh38 chr14: 52,564,934-52,564,934 , GRCh38 chr14: 52,559,510-52,559,510 , GRCh37.p13 chr14: 53,026,228-53,026,228 , GRCh37.p13 chr14: 53,031,652-53,031,652 GPR137C
    nsv5341006translocation1nstd200human GRCh37 chr14: 53,077,047-53,077,047 , GRCh37 chr14: 53,076,980-53,076,980 , GRCh38.p12 chr14: 52,610,262-52,610,262 , GRCh38.p12 chr14: 52,610,329-52,610,329 GPR137C
    nsv5327849translocation1nstd204human GRCh38.p13 chr14: 52,610,329-52,610,329 , GRCh38.p13 chr14: 52,610,262-52,610,262 , GRCh37.p13 chr14: 53,076,980-53,076,980 , GRCh37.p13 chr14: 53,077,047-53,077,047 GPR137C
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