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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5970571inversion1nstd209human GRCh38 chr19: 50,142,503-50,623,829 , GRCh37.p13 chr19: 50,645,760-51,127,086 KCNC3, MYBPC2, 16 more genes
    nsv5381200copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,906,740-50,921,204 , GRCh38.p12 chr19: 50,403,483-50,417,947 POLD1, SPIB
    nsv5381054copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,916,673-50,921,204 , GRCh38.p12 chr19: 50,413,416-50,417,947 POLD1, SPIB
    nsv5325010copy number variation1nstd204human GRCh38.p13 chr19: 50,421,436-50,421,717 , GRCh37.p13 chr19: 50,924,693-50,924,974 SPIB
    nsv5024825copy number variation1nstd200human GRCh38 chr19: 50,425,712-50,426,659 , GRCh37.p13 chr19: 50,928,969-50,929,916 SPIB
    nsv5024824copy number variation1nstd200human GRCh38 chr19: 50,415,934-50,424,618 , GRCh37.p13 chr19: 50,919,191-50,927,875 POLD1, SPIB
    nsv5024823copy number variation1nstd200human GRCh38 chr19: 50,400,018-50,587,989 , GRCh37.p13 chr19: 50,903,275-51,091,246 LRRC4B, EMC10, 6 more genes
    nsv5021044copy number variation1nstd200human GRCh38 chr19: 50,427,787-50,427,889 , GRCh37.p13 chr19: 50,931,044-50,931,146 SPIB
    nsv4865267copy number variation1nstd200human GRCh37 chr19: 50,928,969-50,929,916 , GRCh38.p12 chr19: 50,425,712-50,426,659 SPIB
    nsv4865266copy number variation1nstd200human GRCh37 chr19: 50,903,275-51,091,246 , GRCh38.p12 chr19: 50,400,018-50,587,989 LRRC4B, JOSD2, 6 more genes
    nsv4853379copy number variation1nstd200human GRCh37 chr19: 50,924,709-50,925,072 , GRCh38.p12 chr19: 50,421,452-50,421,815 SPIB
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4683024copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,905,025-50,921,204 , GRCh38.p12 chr19: 50,401,768-50,417,947 POLD1, SPIB
    nsv4682313copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,912,032-50,921,204 , GRCh38.p12 chr19: 50,408,775-50,417,947 POLD1, SPIB
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676347copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,469,730-51,916,485 , GRCh38.p12 chr19: 49,966,473-51,413,231 VRK3, SYT3, 93 more genes
    nsv4628896copy number variation1nstd183human GRCh37 chr19: 50,924,028-50,956,965 , GRCh38.p12 chr19: 50,420,771-50,453,708 MYBPC2, SPIB
    nsv4619315copy number variation1nstd183human GRCh37 chr19: 50,920,243-50,920,336 , GRCh38.p12 chr19: 50,416,986-50,417,079 SPIB, POLD1
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