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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978005insertion1nstd209human GRCh38 chr11: 18,401,955-18,401,955 , GRCh37.p13 chr11: 18,423,502-18,423,502 LDHA
    nsv5971822insertion1nstd209human GRCh38 chr11: 18,401,457-18,401,457 , GRCh37.p13 chr11: 18,423,004-18,423,004 LDHA
    nsv5727780mobile element insertion2nstd211human GRCh38 chr11: 18,401,976-18,401,976 , GRCh37.p13 chr11: 18,423,523-18,423,523 LDHA
    nsv5509381copy number variation1nstd206human GRCh38 chr11: 18,405,323-18,410,980 , GRCh37.p13 chr11: 18,426,870-18,432,527 LDHA, LDHC
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    nsv5507420copy number variation1nstd206human GRCh38 chr11: 18,406,737-18,439,526 , GRCh37.p13 chr11: 18,428,284-18,461,073 LDHC, LDHA
    nsv5496365copy number variation1nstd206human GRCh38 chr11: 18,398,516-18,398,594 , GRCh37.p13 chr11: 18,420,063-18,420,141 LDHA
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5380720copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,552,691-19,213,995 , GRCh38.p12 chr11: 17,531,144-19,192,448 USH1C, HIGD1AP5, 53 more genes
    nsv5379907translocation1nstd200human GRCh38 chr11: 18,407,167-18,407,167 , GRCh38 chr2: 7,040,602-7,040,602 , GRCh37.p13 chr11: 18,428,714-18,428,714 , GRCh37.p13 chr2: 7,180,733-7,180,733 LDHA, RNF144A
    nsv5373458translocation1nstd200human GRCh38 chr11: 18,400,671-18,400,671 , GRCh38 chr11: 18,398,485-18,398,485 , GRCh37.p13 chr11: 18,420,032-18,420,032 , GRCh37.p13 chr11: 18,422,218-18,422,218 LDHA
    nsv5194567mobile element insertion1nstd203human GRCh38 chr11: 18,401,955-18,401,976 , GRCh37.p13 chr11: 18,423,502-18,423,523 LDHA
    nsv5137358mobile element insertion1nstd203human GRCh38 chr11: 18,401,960-18,401,976 , GRCh37.p13 chr11: 18,423,507-18,423,523 LDHA
    nsv4984241copy number variation1nstd200human GRCh38 chr11: 18,404,555-18,414,792 , GRCh37.p13 chr11: 18,426,102-18,436,339 LDHC, LDHA
    nsv4984240copy number variation1nstd200human GRCh38 chr11: 18,366,168-18,410,341 , GRCh37.p13 chr11: 18,387,715-18,431,888 LDHA, LDHC, 2 more genes
    nsv4978463copy number variation1nstd200human GRCh38 chr11: 18,404,407-18,408,930 , GRCh37.p13 chr11: 18,425,954-18,430,477 LDHA
    nsv4841206copy number variation1nstd200human GRCh37 chr11: 18,426,141-18,436,298 , GRCh38.p12 chr11: 18,404,594-18,414,751 LDHA, LDHC
    nsv4832265copy number variation1nstd200human GRCh37 chr11: 18,425,954-18,430,477 , GRCh38.p12 chr11: 18,404,407-18,408,930 LDHA
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
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