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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057082inversion1nstd229human GRCh38 chr5: 139,208,712-142,493,851 , GRCh37.p13 chr5: 138,544,401-141,873,416 SPRY4-AS1, SPRY4, 151 more genes
    nsv6785934copy number variation1nstd229human GRCh38 chr5: 141,174,601-142,728,000 , GRCh37.p13 chr5: 140,687,717-142,107,565 TAF7, RNF14, 64 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
    nsv6559320inversion1nstd223human GRCh38 chr5: 141,304,478-141,304,803 , GRCh37.p13 chr5|NW_004775428.1: 539,654-539,979 , GRCh37.p13 chr5: 140,684,045-140,684,370 SLC25A2
    nsv6406749copy number variation1nstd223human GRCh38 chr5: 141,284,109-141,319,176 , GRCh37.p13 chr5: 140,663,674-140,687,716 , GRCh37.p13 chr5|NW_004775428.1: 519,285-543,325 SLC25A2, TAF7
    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
    nsv6403869copy number variation1nstd223human GRCh38 chr5: 141,059,401-141,554,400 , GRCh37.p13 chr5: 140,438,986-140,687,716 , GRCh37.p13 chr5|NW_004775428.1: 294,577-543,325 PCDHG@, PCDHGC4, 50 more genes
    nsv6398660copy number variation1nstd223human GRCh38 chr5: 141,068,401-141,554,700 , GRCh37.p13 chr5: 140,687,717-140,934,267 PCDHB@, TAF7, 49 more genes
    nsv6395740copy number variation1nstd223human GRCh38 chr5: 141,065,301-141,541,300 , GRCh37.p13 chr5: 140,444,886-140,687,716 , GRCh37.p13 chr5|NW_004775428.1: 300,477-543,325 PCDHGB7, PCDHB@, 49 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
    nsv5470484copy number variation1nstd206human GRCh37.p13 chr5|NW_004775428.1: 487,924-543,345 , GRCh38 chr5: 141,252,748-141,308,652 , GRCh37.p13 chr5: 140,632,316-140,687,736 SLC25A2, LOC100419552, 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
    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
    nsv4945163copy number variation1nstd200human GRCh38 chr5: 141,284,109-141,319,179 , GRCh37.p13 chr5|NW_004775428.1: 519,285-543,325 , GRCh37.p13 chr5: 140,663,674-140,687,716 SLC25A2, TAF7
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4805875copy number variation1nstd200human GRCh37 chr5: 140,663,674-140,698,746 , GRCh38.p12 chr5: 141,284,109-141,319,179 SLC25A2, TAF7
    nsv4804234copy number variation1nstd200human GRCh37 chr5: 140,676,708-140,681,535 , GRCh38.p12 chr5: 141,297,143-141,301,970 SLC25A2
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