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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148188copy number variation1nstd102humanPathogenic GRCh38 chr5: 88,189,536-93,784,597 , GRCh37.p13 chr5: 87,485,353-93,120,303 RPS3AP22, LOC105379078, 49 more genes
    nsv7093269copy number variation1nstd102humanPathogenic GRCh37 chr5: 92,920,819-92,920,882 , GRCh38 chr5: 93,585,113-93,585,176 NR2F1
    nsv7042441inversion1nstd229human GRCh38 chr5: 93,589,200-93,589,262 , GRCh37.p13 chr5: 92,924,906-92,924,968 NR2F1
    nsv6773857copy number variation1nstd229human GRCh38 chr5: 93,497,801-93,583,600 , GRCh37.p13 chr5: 92,833,507-92,919,306 NR2F1, NR2F1-AS1
    nsv6408946copy number variation1nstd223human GRCh38 chr5: 93,587,301-93,589,000 , GRCh37.p13 chr5: 92,923,007-92,924,706 NR2F1
    nsv6399048copy number variation1nstd223human GRCh38 chr5: 93,558,101-93,628,600 , GRCh37.p13 chr5: 92,893,807-92,964,306 ARB2A, NR2F1-AS1, 2 more genes
    nsv6312217copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr5: 92,920,730-92,929,548 , GRCh38.p12 chr5: 93,585,024-93,593,842 NR2F1
    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
    nsv6135200copy number variation1nstd213human GRCh37 chr5: 76,540,000-94,260,001 , GRCh38.p12 chr5: 77,244,175-94,924,296 ACTBP2, ARSB, 200 more genes
    nsv6019852copy number variation1nstd212human GRCh38 chr5: 93,581,676-93,581,737 , GRCh37.p13 chr5: 92,917,382-92,917,443 NR2F1, NR2F1-AS1
    nsv6012281copy number variation1nstd212human GRCh38 chr5: 93,583,276-93,583,336 , GRCh37.p13 chr5: 92,918,982-92,919,042 NR2F1
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4748394copy number variation1nstd199human GRCh37 chr5: 92,918,977-92,919,038 , GRCh38.p12 chr5: 93,583,271-93,583,332 NR2F1
    nsv4738601copy number variation1nstd199human GRCh37 chr5: 92,917,374-92,917,478 , GRCh38.p12 chr5: 93,581,668-93,581,772 NR2F1, NR2F1-AS1
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    nsv4675472copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 87,792,844-109,221,844 , GRCh38.p12 chr5: 88,497,027-109,886,143 CAST, CETN3, 202 more genes
    nsv4675441copy number variation1nstd102humanPathogenic GRCh37 chr5: 92,618,672-93,196,696 , GRCh38.p12 chr5: 93,282,966-93,860,990 NR2F1, ARB2A, 4 more genes
    nsv4593352copy number variation1nstd183human GRCh37 chr5: 92,919,794-92,920,972 , GRCh38.p12 chr5: 93,584,088-93,585,266 NR2F1
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