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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097512copy number variation1nstd102humanUncertain significance GRCh37 chr5: 139,930,285-140,078,137 , GRCh38.p12 chr5: 140,550,700-140,698,552 TMCO6, ZMAT2, 15 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
    nsv7057082inversion1nstd229human GRCh38 chr5: 139,208,712-142,493,851 , GRCh37.p13 chr5: 138,544,401-141,873,416 SPRY4-AS1, SPRY4, 151 more genes
    nsv7043618inversion1nstd229human GRCh38 chr5: 140,515,390-140,897,647 , GRCh37.p13 chr5: 139,894,975-140,144,409 PCDHA1, TMCO6, 39 more genes
    nsv6789654copy number variation1nstd229human GRCh38 chr5: 140,685,566-140,689,701 , GRCh37.p13 chr5: 140,065,151-140,069,286 HARS2, HARS1
    nsv6562823inversion1nstd223human GRCh38 chr5: 140,515,380-140,897,647 , GRCh37.p13 chr5: 139,894,965-140,144,409 HARS2, ANKHD1, 39 more genes
    nsv6410875copy number variation1nstd223human GRCh38 chr5: 140,690,101-140,733,400 , GRCh37.p13 chr5: 140,069,686-140,112,985 VTRNA1-3, HARS2, 5 more genes
    nsv6408594copy number variation1nstd223human GRCh38 chr5: 140,515,601-140,836,000 , GRCh37.p13 chr5: 139,895,186-140,144,409 PCDHA2, RPL36P11, 31 more genes
    nsv6407401copy number variation1nstd223human GRCh38 chr5: 140,339,301-140,944,600 , GRCh37.p13 chr5: 139,718,886-140,144,409 IK, RNU4-14P, 43 more genes
    nsv6405798copy number variation1nstd223human GRCh38 chr5: 140,685,566-140,689,696 , GRCh37.p13 chr5: 140,065,151-140,069,281 HARS1, HARS2
    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
    nsv6296670copy number variation1nstd186human GRCh37 chr5: 140,072,196-140,074,366 , GRCh38.p12 chr5: 140,692,611-140,694,781 HARS2
    nsv6290261copy number variation1nstd102humanPathogenic GRCh37 chr5: 139,493,717-140,517,454 , GRCh38.p12 chr5: 140,114,132-141,137,872 PCDHA2, RPL36P11, 57 more genes
    nsv6244897mobile element insertion1nstd215human GRCh38 chr5: 140,689,550-140,689,550 , GRCh37.p13 chr5: 140,069,135-140,069,135 HARS1, HARS2
    nsv6135653copy number variation1nstd213human GRCh37 chr5: 138,340,000-143,460,001 , GRCh38.p12 chr5: 139,004,311-144,080,436 CD14, DIAPH1, 170 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
    nsv6135117copy number variation1nstd213human GRCh37 chr5: 140,060,000-141,240,001 , GRCh38.p12 chr5: 140,680,415-141,860,436 DIAPH1, HARS1, 85 more genes
    nsv5464010copy number variation1nstd206human GRCh38 chr5: 140,692,611-140,694,781 , GRCh37.p13 chr5: 140,072,196-140,074,366 HARS2
    nsv5381613copy number variation1nstd102humanUncertain significance GRCh37 chr5: 140,052,489-140,072,312 , GRCh38.p12 chr5: 140,672,904-140,692,727 WDR55, DND1, 2 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
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