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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5455624copy number variation1nstd206human GRCh38 chr5: 139,275,347-139,275,931 , GRCh37.p13 chr5: 138,611,036-138,611,620 SNHG4, SNORA74D, 1 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
    nsv5300443copy number variation1nstd204human GRCh37.p13 chr5: 138,611,034-138,611,629 , GRCh38.p13 chr5: 139,275,345-139,275,940 MATR3, SNHG4, 1 more genes
    nsv5086243mobile element insertion1nstd203human GRCh38 chr5: 139,279,907-139,279,926 , GRCh37.p13 chr5: 138,615,596-138,615,615 SNHG4, MATR3
    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
    nsv4945138copy number variation1nstd200human GRCh38 chr5: 139,264,188-139,309,695 , GRCh37.p13 chr5: 138,599,877-138,645,384 MATR3, RNA5SP195, 3 more genes
    nsv4945130copy number variation1nstd200human GRCh38 chr5: 138,884,159-139,363,171 , GRCh37.p13 chr5: 138,219,848-138,698,860 , SNORA74A, 11 more genes
    nsv4938861copy number variation1nstd200human GRCh38 chr5: 139,275,347-139,275,931 , GRCh37.p13 chr5: 138,611,036-138,611,620 MATR3, SNHG4, 1 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4804177copy number variation1nstd200human GRCh37 chr5: 138,611,036-138,611,620 , GRCh38.p12 chr5: 139,275,347-139,275,931 MATR3, SNHG4, 1 more genes
    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
    nsv4597767copy number variation1nstd183human GRCh37 chr5: 138,600,792-138,644,807 , GRCh38.p12 chr5: 139,265,103-139,309,118 MATR3, SNHG4, 3 more genes
    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
    nsv4127374copy number variation1nstd166human GRCh37.p13 chr5: 138,612,259-138,612,344 , GRCh38.p12 chr5: 139,276,570-139,276,655 MATR3, SNHG4, 1 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
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