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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054819inversion1nstd229human GRCh38 chr5: 112,393,108-116,183,657 , GRCh37.p13 chr5: 111,728,805-115,519,354 SRP19, LINCADL, 53 more genes
    nsv7047000inversion1nstd229human GRCh38 chr5: 112,427,651-114,848,458 , GRCh37.p13 chr5: 111,763,348-114,184,155 XBP1P1, SRP19, 23 more genes
    nsv6776637copy number variation1nstd229human GRCh38 chr5: 114,534,560-114,626,566 , GRCh37.p13 chr5: 113,870,257-113,962,263 LOC101927078, LINC01957
    nsv6770283copy number variation1nstd229human GRCh38 chr5: 114,518,100-114,636,056 , GRCh37.p13 chr5: 113,853,797-113,971,753 LINC01957, LOC101927078
    nsv6766592copy number variation1nstd229human GRCh38 chr5: 114,571,550-114,576,991 , GRCh37.p13 chr5: 113,907,247-113,912,688 LOC101927078, LINC01957
    nsv6765749copy number variation1nstd229human GRCh38 chr5: 114,538,433-114,617,112 , GRCh37.p13 chr5: 113,874,130-113,952,809 LOC101927078, LINC01957
    nsv6765644copy number variation1nstd229human GRCh38 chr5: 114,254,766-114,813,380 , GRCh37.p13 chr5: 113,590,463-114,149,077 LOC101927078, LINC01957, 1 more genes
    nsv6761842copy number variation1nstd229human GRCh38 chr5: 114,578,601-114,591,408 , GRCh37.p13 chr5: 113,914,298-113,927,105 LOC101927078, LINC01957
    nsv6759109copy number variation1nstd229human GRCh38 chr5: 114,566,101-114,607,500 , GRCh37.p13 chr5: 113,901,798-113,943,197 LINC01957, LOC101927078
    nsv6637111copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,557,391-128,106,299 , GRCh38.p12 chr5: 113,221,694-128,770,606 SLC12A2, CCDC192, 180 more genes
    nsv6409353copy number variation1nstd223human GRCh38 chr5: 114,579,901-114,582,100 , GRCh37.p13 chr5: 113,915,598-113,917,797 LOC101927078, LINC01957
    nsv6313698copy number variation1nstd102humanPathogenic GRCh37 chr5: 111,443,783-116,255,660 , GRCh38.p12 chr5: 112,108,086-116,919,964 RPS17P2, COMMD10, 71 more genes
    nsv6313580copy number variation1nstd102humanPathogenic GRCh37 chr5: 93,650,000-114,969,108 , GRCh38.p12 chr5: 94,314,295-115,633,411 FER, HMGN1P15, 222 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv5572394copy number variation1nstd207human GRCh38 chr5: 114,500,482-114,659,978 , GRCh37.p13 chr5: 113,836,179-113,995,675 LINC01957, LOC101927078
    nsv5465718copy number variation1nstd206human GRCh38 chr5: 114,500,522-114,659,979 , GRCh37.p13 chr5: 113,836,219-113,995,676 LINC01957, LOC101927078
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4944939copy number variation1nstd200human GRCh38 chr5: 114,554,134-114,577,257 , GRCh37.p13 chr5: 113,889,831-113,912,954 LOC101927078, LINC01957
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