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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
    nsv7075760inversion1nstd229human GRCh38 chr19: 54,368,885-57,042,988 , GRCh37.p13 chr19: 55,595,687-57,554,356 ZSCAN5C, TMEM190, 137 more genes
    nsv7067331inversion1nstd229human GRCh38 chr19: 54,730,353-56,291,074 , GRCh37.p13 chr19: 55,595,687-56,802,443 NLRP2, KIR2DP1, 85 more genes
    nsv7062087inversion1nstd229human GRCh38 chr19: 54,368,882-57,042,981 , GRCh37.p13 chr19: 55,595,687-57,554,349 BRSK1, ZIM2, 137 more genes
    nsv7005862copy number variation1nstd229human GRCh38 chr19: 55,590,452-55,590,484 , GRCh37.p13 chr19: 56,101,818-56,101,850 FIZ1
    nsv6535472copy number variation1nstd223human GRCh38 chr19: 55,592,101-55,594,700 , GRCh37.p13 chr19: 56,103,467-56,106,066 FIZ1
    nsv6524568copy number variation1nstd223human GRCh38 chr19: 55,596,408-55,597,082 , GRCh37.p13 chr19: 56,107,774-56,108,448 FIZ1
    nsv6520388copy number variation1nstd223human GRCh38 chr19: 55,591,301-55,593,900 , GRCh37.p13 chr19: 56,102,667-56,105,266 FIZ1
    nsv6315178copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,434,660-56,463,734 , GRCh38.p12 chr19: 54,923,292-55,952,368 RDH13, SSC5D, 62 more genes
    nsv6291483copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 55,247,893-56,503,347 , GRCh38.p12 chr19: 54,911,986-55,991,981 IL11, PTPRH, 62 more genes
    nsv5324460copy number variation1nstd204human GRCh38.p13 chr19: 55,593,826-55,594,240 , GRCh37.p13 chr19: 56,105,192-56,105,606 FIZ1
    nsv5028094copy number variation1nstd200human GRCh38 chr19: 55,596,408-55,597,082 , GRCh37.p13 chr19: 56,107,774-56,108,448 FIZ1
    nsv4861410copy number variation1nstd200human GRCh37 chr19: 56,107,773-56,108,448 , GRCh38.p12 chr19: 55,596,407-55,597,082 FIZ1
    nsv4861409copy number variation1nstd200human GRCh37 chr19: 56,105,215-56,105,583 , GRCh38.p12 chr19: 55,593,849-55,594,217 FIZ1
    nsv4730034copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,334,195-56,434,037 , GRCh38.p12 chr19: 53,830,941-55,922,671 , GRCh38.p12 chr19|NT_187693.1: 1-1,066,800 , GRCh38.p12 chr19|NW_003571057.2: 1-1,091,841 , GRCh38.p12 chr19|NW_003571058.2: 1-1,066,390 , GRCh38.p12 chr19|NW_003571056.2: 1-1,064,304 KIR3DP1, NLRP9, 133 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
    nsv4392420copy number variation1nstd171human GRCh37 chr19: 56,101,816-56,101,846 , GRCh38.p12 chr19: 55,590,450-55,590,480 FIZ1
    nsv4272097copy number variation1nstd166human GRCh37.p13 chr19: 56,107,774-56,108,448 , GRCh38.p12 chr19: 55,596,408-55,597,082 FIZ1
    nsv3929209copy number variation1nstd167human GRCh37 chr19: 56,101,815-56,101,846 , GRCh38.p12 chr19: 55,590,449-55,590,480 FIZ1
    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
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