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Items: 1 to 20 of 1013

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121296copy number variation1nstd186human GRCh37 chr9: 136,130,254-136,130,422 , GRCh38.p12 chr9|NW_009646201.1: 80,858-81,128 , GRCh38.p12 chr9: 133,254,867-133,255,035 ABO
    nsv5388881copy number variation1nstd186human GRCh37 chr9: 136,065,756-136,065,942 , GRCh38.p12 chr9|NW_009646201.1: 16,315-16,501 , GRCh38.p12 chr9: 133,190,369-133,190,555 0
    nsv5388842copy number variation2nstd186human GRCh37 chr9: 136,172,546-136,172,713 , GRCh38.p12 chr9|NW_009646201.1: 123,065-123,232 , GRCh38.p12 chr9: 133,296,971-133,297,138 0
    nsv5384892mobile element deletion2nstd186human GRCh37 chr9: 136,060,728-136,061,032 , GRCh38.p12 chr9: 133,185,341-133,185,645 , GRCh38.p12 chr9|NW_009646201.1: 11,287-11,591 0
    nsv5344201translocation1nstd200human GRCh37 chr9: 136,170,929-136,170,929 , GRCh37 chr9: 136,176,704-136,176,704 , GRCh38.p12 chr9: 133,295,357-133,295,357 , GRCh38.p12 chr9|NW_009646201.1: 121,451-121,451 , GRCh38.p12 chr9: 133,301,221-133,301,221 , GRCh38.p12 chr9|NW_009646201.1: 127,315-127,315 0
    nsv5343309translocation1nstd200human GRCh37 chr9: 136,261,558-136,261,558 , GRCh37 chr9: 136,261,626-136,261,626 , GRCh38.p12 chr9: 133,396,499-133,396,499 , GRCh38.p12 chr9: 133,396,431-133,396,431 , GRCh38.p12 chr9|NW_009646201.1: 222,593-222,593 , GRCh38.p12 chr9|NW_009646201.1: 222,525-222,525 STKLD1
    nsv5340880translocation1nstd200human GRCh37 chr9: 136,080,054-136,080,054 , GRCh37 chr9: 136,184,253-136,184,253 , GRCh38.p12 chr9: 133,204,667-133,204,667 , GRCh38.p12 chr9: 133,317,418-133,317,418 , GRCh38.p12 chr9|NW_009646201.1: 143,512-143,512 , GRCh38.p12 chr9|NW_009646201.1: 30,613-30,613 LCN1, OBP2B, 1 more genes
    nsv5329737translocation1nstd200human GRCh37 chr9: 136,080,089-136,080,089 , GRCh37 chr9: 136,026,349-136,026,349 , GRCh38.p12 chr9: 133,150,962-133,150,962 , GRCh38.p12 chr9: 133,204,702-133,204,702 , GRCh38.p12 chr9|NW_009646201.1: 30,648-30,648 OBP2B, GBGT1
    nsv4848342copy number variation1nstd200human GRCh37 chr9: 136,065,686-136,066,068 , GRCh38.p12 chr9: 133,190,299-133,190,681 , GRCh38.p12 chr9|NW_009646201.1: 16,245-16,627 0
    nsv4848195copy number variation1nstd200human GRCh37 chr9: 136,127,803-136,133,621 , GRCh38.p12 chr9|NW_009646201.1: 78,375-84,324 , GRCh38.p12 chr9: 133,252,416-133,258,230 ABO
    nsv4846534copy number variation1nstd200human GRCh37 chr9: 136,172,546-136,172,713 , GRCh38.p12 chr9|NW_009646201.1: 123,065-123,232 , GRCh38.p12 chr9: 133,296,971-133,297,138 0
    nsv4846518copy number variation1nstd200human GRCh37 chr9: 136,251,919-136,254,252 , GRCh38.p12 chr9: 133,386,135-133,388,468 , GRCh38.p12 chr9|NW_009646201.1: 212,229-214,562 STKLD1
    nsv4843613copy number variation1nstd200human GRCh37 chr9: 136,210,775-136,211,970 , GRCh38.p12 chr9: 133,343,920-133,345,115 , GRCh38.p12 chr9|NW_009646201.1: 170,014-171,209 MED22
    nsv4842194copy number variation1nstd200human GRCh37 chr9: 136,059,924-136,061,904 , GRCh38.p12 chr9|NW_009646201.1: 10,483-12,463 , GRCh38.p12 chr9: 133,184,537-133,186,517 0
    nsv4842121copy number variation1nstd200human GRCh37 chr9: 136,131,701-136,131,783 , GRCh38.p12 chr9: 133,256,314-133,256,396 , GRCh38.p12 chr9|NW_009646201.1: 82,407-82,489 ABO
    nsv4841414copy number variation1nstd200human GRCh37 chr9: 136,295,878-136,299,707 , GRCh38.p12 chr9: 133,430,758-133,434,587 , GRCh38.p12 chr9|NW_009646201.1: 256,852-260,681 ADAMTS13
    nsv4841085copy number variation1nstd200human GRCh37 chr9: 136,296,006-136,296,940 , GRCh38.p12 chr9|NW_009646201.1: 256,980-257,913 , GRCh38.p12 chr9: 133,430,886-133,431,819 ADAMTS13
    nsv4839135copy number variation1nstd200human GRCh37 chr9: 136,176,787-136,178,726 , GRCh38.p12 chr9: 133,301,304-133,303,243 , GRCh38.p12 chr9|NW_009646201.1: 127,398-129,337 0
    nsv4837150copy number variation1nstd200human GRCh37 chr9: 136,095,747-136,096,986 , GRCh38.p12 chr9: 133,220,360-133,221,599 , GRCh38.p12 chr9|NW_009646201.1: 46,306-47,545 OBP2B
    nsv4835612copy number variation1nstd200human GRCh37 chr9: 136,169,548-136,170,924 , GRCh38.p12 chr9: 133,293,976-133,295,352 , GRCh38.p12 chr9|NW_009646201.1: 120,070-121,446 0
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