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Items: 1 to 20 of 79

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077997inversion1nstd229human GRCh38 chr19: 50,085,764-53,270,581 , GRCh37.p13 chr19: 50,589,021-53,773,834 SNORD88B, ZNF320, 181 more genes
    nsv7075255inversion1nstd229human GRCh38 chr19: 49,270,356-54,089,823 , GRCh37.p13 chr19: 49,773,613-54,528,887 FPR2, SNAR-A11, 344 more genes
    nsv7069681inversion1nstd229human GRCh38 chr19: 50,654,313-52,443,676 , GRCh37.p13 chr19: 51,157,570-52,946,929 CTU1, LOC100419835, 117 more genes
    nsv7064925inversion1nstd229human GRCh38 chr19: 49,540,460-54,108,860 , GRCh37.p13 chr19: 50,043,717-54,528,887 DPRX, EMC10, 323 more genes
    nsv7062200inversion1nstd229human GRCh38 chr19: 51,156,828-51,481,685 , GRCh37.p13 chr19: 51,660,085-51,984,939 VSIG10L, SIGLEC20P, 27 more genes
    nsv6998345copy number variation1nstd229human GRCh38 chr19: 51,170,801-51,179,700 , GRCh37.p13 chr19: 51,674,058-51,682,956 SIGLEC17P, LOC101928517
    nsv6637793copy number variation1nstd102humanUncertain significance GRCh37 chr19: 51,623,330-51,694,022 , GRCh38.p12 chr19: 51,120,073-51,190,766 SIGLEC9, SIGLEC20P, 4 more genes
    nsv6625270copy number variation1nstd224human GRCh37 chr19: 51,659,922-51,706,621 , GRCh38.p12 chr19: 51,156,665-51,203,365 SIGLEC20P, SIGLEC17P, 3 more genes
    nsv6532706copy number variation1nstd223human GRCh38 chr19: 51,168,346-51,212,096 , GRCh37.p13 chr19: 51,671,603-51,715,352 SIGLEC17P, MIR8074, 6 more genes
    nsv6313906copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 49,911,081-53,127,438 , GRCh38.p12 chr19: 49,407,824-52,624,185 AP2A1, KLK3, 212 more genes
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 more genes
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5524747copy number variation1nstd206human GRCh38 chr19: 51,173,028-51,173,088 , GRCh37.p13 chr19: 51,676,285-51,676,345 LOC101928517, SIGLEC17P
    nsv5024840copy number variation1nstd200human GRCh38 chr19: 51,168,342-51,212,181 , GRCh37.p13 chr19: 51,671,599-51,715,437 SIGLEC22P, SIGLEC17P, 6 more genes
    nsv4865275copy number variation1nstd200human GRCh37 chr19: 51,671,561-51,715,456 , GRCh38.p12 chr19: 51,168,304-51,212,200 LOC101928517, SIGLEC20P, 6 more genes
    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
    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
    nsv4540475insertion1nstd166human GRCh37.p13 chr19: 51,672,560-51,672,560 , GRCh38.p12 chr19: 51,169,303-51,169,303 LOC101928517, SIGLEC17P
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