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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906316copy number variation1nstd209human GRCh38 chr5: 137,872,471-137,872,607 , GRCh37.p13 chr5: 137,208,160-137,208,296 MYOT, PKD2L2-DT
    nsv5898795copy number variation1nstd209human GRCh38 chr5: 137,868,839-137,868,955 , GRCh37.p13 chr5: 137,204,528-137,204,644 PKD2L2-DT, MYOT
    nsv5675457mobile element insertion2nstd211human GRCh38 chr5: 137,883,252-137,883,252 , GRCh37.p13 chr5: 137,218,941-137,218,941 MYOT, PKD2L2-DT
    nsv5643385insertion1nstd207human GRCh38 chr5: 137,868,839-137,868,839 , GRCh37.p13 chr5: 137,204,528-137,204,528 PKD2L2-DT, MYOT
    nsv5633551insertion1nstd207human GRCh38 chr5: 137,883,231-137,883,231 , GRCh37.p13 chr5: 137,218,920-137,218,920 MYOT, PKD2L2-DT
    nsv5471050copy number variation1nstd206human GRCh38 chr5: 137,856,777-138,124,570 , GRCh37.p13 chr5: 137,192,466-137,460,259 RNU6-460P, RNU6-1148P, 9 more genes
    nsv5463969copy number variation1nstd206human GRCh38 chr5: 137,868,839-137,868,956 , GRCh37.p13 chr5: 137,204,528-137,204,645 MYOT, PKD2L2-DT
    nsv5407172mobile element insertion1nstd206human GRCh38 chr5: 137,883,252-137,883,303 , GRCh37.p13 chr5: 137,218,941-137,218,992 PKD2L2-DT, MYOT
    nsv5381777copy number variation1nstd102humanPathogenic GRCh37 chr5: 136,409,875-137,739,167 , GRCh38.p12 chr5: 137,074,186-138,403,478 HNRNPA0, SPOCK1, 24 more genes
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 RNA5SP195, LOC112267855, 174 more genes
    nsv5302092copy number variation1nstd204human GRCh38.p13 chr5: 137,856,772-138,124,571 , GRCh37.p13 chr5: 137,192,461-137,460,260 RNU6-1148P, PKD2L2-DT, 9 more genes
    nsv5227191copy number variation1nstd204human GRCh38.p13 chr5: 137,856,739-137,863,138 , GRCh37.p13 chr5: 137,192,428-137,198,827 LOC107986368, PKD2L2-DT
    nsv5095996mobile element insertion1nstd203human GRCh38 chr5: 137,860,679-137,860,681 , GRCh37.p13 chr5: 137,196,368-137,196,370 LOC107986368, PKD2L2-DT
    nsv5091456mobile element insertion1nstd203human GRCh38 chr5: 137,883,234-137,883,252 , GRCh37.p13 chr5: 137,218,923-137,218,941 PKD2L2-DT, MYOT
    nsv5080186mobile element insertion1nstd203human GRCh38 chr5: 137,883,231-137,883,252 , GRCh37.p13 chr5: 137,218,920-137,218,941 MYOT, PKD2L2-DT
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 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
    nsv4945115copy number variation1nstd200human GRCh38 chr5: 137,856,777-138,124,570 , GRCh37.p13 chr5: 137,192,466-137,460,259 RNU6-1148P, FAM13B, 9 more genes
    nsv4938811copy number variation1nstd200human GRCh38 chr5: 137,863,182-137,864,189 , GRCh37.p13 chr5: 137,198,871-137,199,878 PKD2L2-DT
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
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