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Items: 1 to 20 of 111

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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
    nsv5942909copy number variation1nstd209human GRCh38 chr19: 51,709,917-51,720,828 , GRCh37.p13 chr19: 52,213,170-52,224,081 HAS1, SPACA6
    nsv5869023copy number variation1nstd209human GRCh38 chr19: 51,709,888-51,720,871 , GRCh37.p13 chr19: 52,213,141-52,224,124 SPACA6, HAS1
    nsv5024846copy number variation1nstd200human GRCh38 chr19: 51,721,256-51,857,363 , GRCh37.p13 chr19: 52,224,509-52,360,616 FPR2, HAS1, 5 more genes
    nsv4865279copy number variation1nstd200human GRCh37 chr19: 52,224,509-52,360,616 , GRCh38.p12 chr19: 51,721,256-51,857,363 FPR1, LOC105372448, 5 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
    nsv4267614copy number variation1nstd166human GRCh37.p13 chr19: 52,186,589-52,302,515 , GRCh38.p12 chr19: 51,683,336-51,799,262 HAS1, SPACA6, 8 more genes
    nsv4262665copy number variation1nstd166human GRCh37.p13 chr19: 52,224,451-52,360,616 , GRCh38.p12 chr19: 51,721,198-51,857,363 FPR1, FPR2, 5 more genes
    nsv4254966copy number variation1nstd166human GRCh37.p13 chr19: 52,218,304-52,220,704 , GRCh38.p12 chr19: 51,715,051-51,717,451 HAS1
    nsv3924732copy number variation1nstd102humanPathogenic GRCh38 chr19: 49,907,832-58,557,889 , GRCh37 chr19: 50,411,089-59,069,256 , NCBI36 chr19: 55,102,901-63,761,068 RPL39P37, CCDC106, 556 more genes
    nsv3923909copy number variation1nstd102humanPathogenic NCBI36 chr19: 55,347,589-63,784,382 , GRCh37 chr19: 50,655,777-59,092,570 , GRCh38 chr19: 50,152,520-58,581,203 OSCAR, FKBP1AP1, 535 more genes
    nsv3922599copy number variation1nstd102humanPathogenic GRCh38 chr19: 51,141,518-58,539,965 , NCBI36 chr19: 56,336,587-63,743,144 , GRCh37 chr19: 51,644,775-59,051,332 LOC100421130, A1BG-AS1, 475 more genes
    nsv3919076copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206 KCNA7, ZNF28, 697 more genes
    nsv3916611copy number variation1nstd102humanPathogenic GRCh37 chr19: 50,694,476-59,047,185 , NCBI36 chr19: 55,386,288-63,738,997 , GRCh38 chr19: 50,191,219-58,535,818 RNU6-980P, ERVV-1, 526 more genes
    nsv3914269copy number variation1nstd102humanUncertain significance GRCh38 chr19: 51,202,361-51,993,020 , NCBI36 chr19: 56,397,429-57,188,085 , GRCh37 chr19: 51,705,617-52,496,273 NIFKP6, HAS1, 54 more genes
    nsv3914123copy number variation1nstd102humanLikely benign NCBI36 chr19: 56,876,300-57,131,488 , GRCh38 chr19: 51,681,235-51,936,423 , GRCh37 chr19: 52,184,488-52,439,676 ZNF649, VN1R98P, 15 more genes
    nsv3911950copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,411,797-59,051,332 , NCBI36 chr19: 53,103,609-63,743,144 , GRCh38 chr19: 47,908,540-58,539,965 LOC107987270, MIR6799, 694 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
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