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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5840290copy number variation1nstd209human GRCh38 chr5: 103,102,769-103,104,668 , GRCh37.p13 chr5|NW_003871061.1: 17,636-19,535 , GRCh37.p13 chr5: 102,438,473-102,440,372 GIN1
    nsv5535441insertion1nstd206human GRCh38 chr5: 103,118,776-103,118,816 , GRCh37.p13 chr5|NW_003871061.1: 33,643-33,683 , GRCh37.p13 chr5: 102,454,480-102,454,520 GIN1, PPIP5K2
    nsv5080369mobile element insertion1nstd203human GRCh38 chr5: 103,112,277-103,112,291 , GRCh37.p13 chr5|NW_003871061.1: 27,144-27,158 , GRCh37.p13 chr5: 102,447,981-102,447,995 GIN1
    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
    nsv4931880copy number variation1nstd200human GRCh38 chr5: 103,084,435-103,086,624 , GRCh37.p13 chr5|NW_003871061.1: 1-1,491 , GRCh37.p13 chr5: 102,420,838-102,422,328 GIN1
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4793566copy number variation1nstd200human GRCh37 chr5: 102,425,822-102,426,893 , GRCh38.p12 chr5: 103,090,118-103,091,189 GIN1
    nsv4728860copy number variation1nstd102humanUncertain significance GRCh37 chr5: 102,034,608-102,540,865 , GRCh38.p12 chr5: 102,698,904-103,205,164 PAM, LOC105379105, 4 more genes
    nsv4724143insertion1nstd186human GRCh37 chr5: 102,454,477-102,454,477 , GRCh38.p12 chr5: 103,118,773-103,118,773 PPIP5K2, GIN1
    nsv4679759copy number variation1nstd189human GRCh37.p13 chr5: 101,552,113-103,688,065 , GRCh38.p12 chr5: 102,216,409-104,352,364 PAM, PPIP5K2, 18 more genes
    nsv4675896copy number variation1nstd102humanUncertain significance GRCh37 chr5: 101,152,187-103,638,623 , GRCh38.p12 chr5: 101,816,483-104,302,922 LOC101930276, NUDT12, 21 more genes
    nsv4675472copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 87,792,844-109,221,844 , GRCh38.p12 chr5: 88,497,027-109,886,143 CAST, CETN3, 202 more genes
    nsv4674820copy number variation1nstd102humanLikely benign GRCh37 chr5: 101,620,402-102,584,810 , GRCh38.p12 chr5: 102,284,698-103,249,109 LINC00491, LOC105379104, 9 more genes
    nsv4589565copy number variation1nstd183human GRCh37 chr5: 102,398,234-102,431,274 , GRCh38.p12 chr5: 103,062,530-103,095,570 LOC105379105, GIN1
    nsv4557179insertion1nstd166human GRCh37.p13 chr5: 102,454,477-102,454,477 , GRCh38.p12 chr5: 103,118,773-103,118,773 PPIP5K2, GIN1
    nsv4456876copy number variation2nstd102humanUncertain significance GRCh37 chr5: 102,096,690-102,460,794 , GRCh38.p12 chr5: 102,760,986-103,125,090 GIN1, EIF3KP1, 3 more genes
    nsv4455983copy number variation1nstd102humanPathogenic GRCh37 chr5: 89,949,118-129,317,455 , GRCh38.p12 chr5: 90,653,301-129,981,762 LOC345576, LOC107986436, 419 more genes
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