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Items: 1 to 20 of 88

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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
    nsv7017789copy number variation1nstd229human GRCh38 chr19: 51,591,017-51,591,144 , GRCh37.p13 chr19: 52,094,270-52,094,397 LINC01530, ZNF175
    nsv7013345copy number variation1nstd229human GRCh38 chr19: 51,568,077-51,634,207 , GRCh37.p13 chr19: 52,071,330-52,137,460 ZNF175, SIGLEC5, 3 more genes
    nsv7011788copy number variation1nstd229human GRCh38 chr19: 51,589,362-51,603,308 , GRCh37.p13 chr19: 52,092,615-52,106,561 LOC339352, ZNF175, 1 more genes
    nsv7004543copy number variation1nstd229human GRCh38 chr19: 51,588,559-51,592,793 , GRCh37.p13 chr19: 52,091,812-52,096,046 LINC01530, ZNF175
    nsv6532183copy number variation1nstd223human GRCh38 chr19: 51,577,830-51,591,929 , GRCh37.p13 chr19: 52,081,083-52,095,182 LINC01530, ZNF175
    nsv6531889copy number variation1nstd223human GRCh38 chr19: 51,577,834-51,591,899 , GRCh37.p13 chr19: 52,081,087-52,095,152 LINC01530, ZNF175
    nsv6531069copy number variation1nstd223human GRCh38 chr19: 51,594,838-51,597,234 , GRCh37.p13 chr19: 52,098,091-52,100,487 LOC339352, LINC01530
    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
    nsv6291759copy number variation1nstd102humanUncertain significance GRCh37 chr19: 51,769,834-52,415,762 , GRCh38.p12 chr19: 51,266,580-51,912,509 ZNF649-AS1, SIGLEC12, 46 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
    nsv5024844copy number variation1nstd200human GRCh38 chr19: 51,577,703-51,591,927 , GRCh37.p13 chr19: 52,080,956-52,095,180 ZNF175, LINC01530
    nsv5021108copy number variation1nstd200human GRCh38 chr19: 51,568,081-51,634,207 , GRCh37.p13 chr19: 52,071,334-52,137,460 RPL9P33, LINC01530, 3 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
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