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Items: 1 to 20 of 310

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5335310translocation1nstd200human GRCh37 chr5: 33,949,046-33,949,046 , GRCh37 chr5: 33,949,144-33,949,144 , GRCh38.p12 chr5: 33,949,039-33,949,039 , GRCh38.p12 chr5|NT_187551.1: 150,263-150,263 , GRCh38.p12 chr5: 33,948,941-33,948,941 , GRCh38.p12 chr5|NT_187551.1: 150,361-150,361 SLC45A2
    nsv4802474copy number variation1nstd200human GRCh37 chr5: 33,943,905-33,944,028 , GRCh38.p12 chr5: 33,943,800-33,943,923 , GRCh38.p12 chr5|NT_187551.1: 145,122-145,245 SLC45A2
    nsv4802473copy number variation1nstd200human GRCh37 chr5: 33,931,169-33,931,828 , GRCh38.p12 chr5|NT_187551.1: 132,386-133,045 , GRCh38.p12 chr5: 33,931,064-33,931,723 0
    nsv4802472copy number variation1nstd200human GRCh37 chr5: 33,931,098-33,931,284 , GRCh38.p12 chr5|NT_187551.1: 132,315-132,501 , GRCh38.p12 chr5: 33,930,993-33,931,179 0
    nsv4802471copy number variation1nstd200human GRCh37 chr5: 33,912,406-33,920,146 , GRCh38.p12 chr5: 33,912,301-33,920,041 , GRCh38.p12 chr5|NT_187551.1: 113,623-121,363 0
    nsv4769143insertion1nstd186human GRCh37 chr5: 33,827,273-33,827,273 , GRCh38.p12 chr5: 33,827,168-33,827,168 , GRCh38.p12 chr5|NT_187551.1: 26,504-26,504 ADAMTS12
    nsv4755257insertion1nstd199human GRCh37 chr5: 33,849,072-33,849,072 , GRCh38.p12 chr5: 33,848,967-33,848,967 , GRCh38.p12 chr5|NT_187551.1: 50,301-50,301 ADAMTS12
    nsv4753474insertion1nstd199human GRCh37 chr5: 33,827,268-33,827,268 , GRCh38.p12 chr5: 33,827,163-33,827,163 , GRCh38.p12 chr5|NT_187551.1: 26,499-26,499 ADAMTS12
    nsv4685413insertion1nstd194human GRCh37 chr5: 33,827,273-33,827,273 , GRCh38.p12 chr5: 33,827,168-33,827,168 , GRCh38.p12 chr5|NT_187551.1: 26,504-26,504 ADAMTS12
    nsv4561849mobile element insertion1nstd166human GRCh37.p13 chr5: 33,837,191-33,837,191 , GRCh38.p12 chr5|NT_187551.1: 38,420-38,420 , GRCh38.p12 chr5: 33,837,086-33,837,086 ADAMTS12
    nsv4558352mobile element insertion1nstd166human GRCh37.p13 chr5: 33,852,383-33,852,383 , GRCh38.p12 chr5: 33,852,278-33,852,278 , GRCh38.p12 chr5|NT_187551.1: 53,597-53,597 ADAMTS12
    nsv4478119mobile element insertion1nstd166human GRCh37.p13 chr5: 33,955,934-33,955,934 , GRCh38.p12 chr5: 33,955,829-33,955,829 , GRCh38.p12 chr5|NT_187551.1: 157,151-157,151 SLC45A2
    nsv4478118mobile element insertion1nstd166human GRCh37.p13 chr5: 33,833,594-33,833,594 , GRCh38.p12 chr5: 33,833,489-33,833,489 , GRCh38.p12 chr5|NT_187551.1: 34,847-34,847 ADAMTS12
    nsv4477463mobile element insertion1nstd166human GRCh37.p13 chr5: 33,938,354-33,938,354 , GRCh38.p12 chr5|NT_187551.1: 139,571-139,571 , GRCh38.p12 chr5: 33,938,249-33,938,249 RXFP3
    nsv4477462mobile element insertion1nstd166human GRCh37.p13 chr5: 33,839,803-33,839,803 , GRCh38.p12 chr5: 33,839,698-33,839,698 , GRCh38.p12 chr5|NT_187551.1: 41,033-41,033 ADAMTS12
    nsv4131557copy number variation1nstd166human GRCh37.p13 chr5: 33,873,600-33,873,854 , GRCh38.p12 chr5|NT_187551.1: 74,820-75,074 , GRCh38.p12 chr5: 33,873,495-33,873,749 ADAMTS12
    nsv4129801copy number variation1nstd166human GRCh37.p13 chr5: 33,926,438-33,926,523 , GRCh38.p12 chr5|NT_187551.1: 127,655-127,740 , GRCh38.p12 chr5: 33,926,333-33,926,418 0
    nsv4125446copy number variation1nstd166human GRCh37.p13 chr5: 33,931,169-33,931,828 , GRCh38.p12 chr5|NT_187551.1: 132,386-133,045 , GRCh38.p12 chr5: 33,931,064-33,931,723 0
    nsv4124062copy number variation1nstd166human GRCh37.p13 chr5: 33,881,855-33,881,914 , GRCh38.p12 chr5: 33,881,750-33,881,809 , GRCh38.p12 chr5|NT_187551.1: 83,073-83,132 ADAMTS12
    nsv4119530copy number variation1nstd166human GRCh37.p13 chr5: 33,923,502-33,923,683 , GRCh38.p12 chr5|NT_187551.1: 124,719-124,900 , GRCh38.p12 chr5: 33,923,397-33,923,578 0
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