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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5304757copy number variation1nstd204human GRCh37.p13 chr5: 138,862,746-138,864,915 , GRCh38.p13 chr5: 139,483,161-139,485,330 LOC101059986, STING1
    nsv5096569mobile element insertion1nstd203human GRCh38 chr5: 139,479,848-139,479,853 , GRCh37.p13 chr5: 138,859,433-138,859,438 STING1
    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
    nsv4938876copy number variation1nstd200human GRCh38 chr5: 139,483,155-139,485,346 , GRCh37.p13 chr5: 138,862,740-138,864,931 STING1, LOC101059986
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4804186copy number variation1nstd200human GRCh37 chr5: 138,862,754-138,864,907 , GRCh38.p12 chr5: 139,483,169-139,485,322 LOC101059986, STING1
    nsv4769371copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 137,754,277-138,994,590 , GRCh38.p12 chr5: 138,418,588-139,615,005 CTNNA1, EGR1, 36 more genes
    nsv4729564copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,351,402-138,893,343 , GRCh38.p12 chr5: 139,015,713-139,513,758 PROB1, SNORA74A, 19 more genes
    nsv4729431copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,101,724-138,876,953 , GRCh38.p12 chr5: 138,766,035-139,497,368 PROB1, NCOA4P4, 22 more genes
    nsv4682278copy number variation2nstd102humanUncertain significance GRCh37 chr5: 138,855,826-138,861,309 , GRCh38.p12 chr5: 139,476,241-139,481,724 LOC101059986, STING1
    nsv4456012copy number variation1nstd102humanPathogenic GRCh37 chr5: 137,865,800-139,097,368 , GRCh38.p12 chr5: 138,530,111-139,717,783 SNORD63, ECSCR, 36 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
    nsv3924309copy number variation1nstd102humanPathogenic GRCh37 chr5: 138,206,826-145,191,872 , GRCh38 chr5: 138,871,137-145,812,309 , NCBI36 chr5: 138,234,725-145,172,065 FCHSD1, LOC105378208, 183 more genes
    nsv3923450copy number variation1nstd102humanPathogenic GRCh37 chr5: 137,172,371-140,075,946 , NCBI36 chr5: 137,200,270-140,056,130 , GRCh38 chr5: 137,836,682-140,696,361 RNU6-236P, FAM13B, 89 more genes
    nsv3923414copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811 HNRNPA3P7, RNU6-456P, 514 more genes
    nsv3918919copy number variation1nstd102humanPathogenic GRCh37 chr5: 138,487,100-138,873,213 , GRCh38 chr5: 139,151,411-139,493,628 , NCBI36 chr5: 138,514,999-138,853,397 SLC23A1, MZB1, 18 more genes
    nsv3915579copy number variation1nstd102humanUncertain significance NCBI36 chr5: 138,466,996-139,043,063 , GRCh38 chr5: 139,103,408-139,683,294 , GRCh37 chr5: 138,439,097-139,062,879 MATR3, ECSCR, 23 more genes
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