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Items: 1 to 20 of 87

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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
    nsv6562823inversion1nstd223human GRCh38 chr5: 140,515,380-140,897,647 , GRCh37.p13 chr5: 139,894,965-140,144,409 HARS2, ANKHD1, 39 more genes
    nsv6561687inversion1nstd223human GRCh38 chr5: 140,629,792-140,630,054 , GRCh37.p13 chr5: 140,009,377-140,009,639 CD14, TMCO6
    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
    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
    nsv5454825copy number variation1nstd206human GRCh38 chr5: 140,633,060-140,633,964 , GRCh37.p13 chr5: 140,012,645-140,013,549 TMCO6, CD14
    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
    nsv4938912copy number variation1nstd200human GRCh38 chr5: 140,633,327-140,634,290 , GRCh37.p13 chr5: 140,012,912-140,013,875 TMCO6, CD14
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4455072copy number variation1nstd102humanUncertain significance GRCh37 chr5: 139,447,779-140,047,037 , GRCh38.p12 chr5: 140,068,194-140,667,452 LOC112267855, RNU4-14P, 23 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
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