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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097022copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-138,861,289 , GRCh38.p12 chr5: 137,622,098-139,481,704 CDC25C, SLC23A1, 55 more genes
    nsv7096751copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-140,078,137 , GRCh38.p12 chr5: 137,622,098-140,698,552 CDC25C, LOC100128966, 94 more genes
    nsv6794471copy number variation1nstd229human GRCh38 chr5: 138,464,901-138,467,900 , GRCh37.p13 chr5: 137,800,590-137,803,589 EGR1
    nsv6793835copy number variation1nstd229human GRCh38 chr5: 138,039,501-138,538,500 , GRCh37.p13 chr5: 137,375,190-137,874,189 RNU6-460P, RNU6-1148P, 17 more genes
    nsv6786663copy number variation1nstd229human GRCh38 chr5: 138,469,701-138,481,100 , GRCh37.p13 chr5: 137,805,390-137,816,789 RPL7P19, EGR1
    nsv6405600copy number variation1nstd223human GRCh38 chr5: 137,606,101-142,582,700 , GRCh37.p13 chr5: 136,941,790-141,962,265 TMCO6, PCDHB17P, 191 more genes
    nsv6135383copy number variation1nstd213human GRCh37 chr5: 137,050,000-138,100,001 , GRCh38.p12 chr5: 137,714,311-138,764,312 CDC25C, CTNNA1, 32 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
    nsv6135115copy number variation1nstd213human GRCh37 chr5: 137,330,000-138,340,001 , GRCh38.p12 chr5: 137,994,311-139,004,312 HSPA9, KIF20A, 27 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
    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
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 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
    nsv4592535copy number variation1nstd183human GRCh37 chr5: 137,804,884-137,815,469 , GRCh38.p12 chr5: 138,469,195-138,479,780 EGR1, RPL7P19
    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
    nsv4400255copy number variation1nstd174human GRCh37 chr5: 137,801,533-137,818,916 , GRCh38.p12 chr5: 138,465,844-138,483,227 EGR1, RPL7P19
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
    nsv3956834copy number variation1nstd168human GRCh38 chr5: 138,464,223-138,482,506 , GRCh37.p13 chr5: 137,799,912-137,818,195 RPL7P19, EGR1
    nsv3924452copy number variation1nstd102humanUncertain significance GRCh37 chr5: 137,515,583-138,375,579 , GRCh38 chr5: 138,179,894-139,039,890 , NCBI36 chr5: 137,543,482-138,403,478 HSPA9, CDC23, 21 more genes
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