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Items: 1 to 20 of 104

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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
    nsv6636350copy number variation1nstd102humanUncertain significance GRCh37 chr5: 140,082,762-140,773,954 , GRCh38.p12 chr5: 140,703,177-141,394,387 PCDHA13, PCDHA10, 61 more genes
    nsv6562823inversion1nstd223human GRCh38 chr5: 140,515,380-140,897,647 , GRCh37.p13 chr5: 139,894,965-140,144,409 HARS2, ANKHD1, 39 more genes
    nsv6413198copy number variation1nstd223human GRCh38 chr5: 140,706,996-140,708,150 , GRCh37.p13 chr5: 140,086,581-140,087,735 ZMAT2
    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
    nsv6409195copy number variation1nstd223human GRCh38 chr5: 140,706,901-140,811,900 , GRCh37.p13 chr5: 140,086,486-140,144,409 ZMAT2, LOC100421074, 9 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
    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
    nsv6400865copy number variation1nstd223human GRCh38 chr5: 140,707,119-140,716,799 , GRCh37.p13 chr5: 140,086,704-140,096,384 LOC105378198, ZMAT2, 1 more genes
    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
    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
    nsv5894175copy number variation1nstd209human GRCh38 chr5: 140,704,745-140,862,604 , GRCh37.p13 chr5: 140,144,410-140,242,189 , GRCh37.p13 chr5|NW_004775428.1: 1-97,780 VTRNA1-2, PCDHA@, 16 more genes
    nsv5841780copy number variation1nstd209human GRCh38 chr5: 140,704,810-140,711,997 , GRCh37.p13 chr5: 140,084,395-140,091,582 ZMAT2, VTRNA1-1, 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
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