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Items: 1 to 20 of 215

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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
    nsv7010659copy number variation1nstd229human GRCh38 chr19: 52,029,683-52,029,711 , GRCh37.p13 chr19: 52,532,936-52,532,964 ZNF432, LOC112268244
    nsv7001828copy number variation1nstd229human GRCh38 chr19: 51,768,552-52,114,483 , GRCh37.p13 chr19: 52,271,805-52,617,736 FPR2, ZNF577, 17 more genes
    nsv6625271copy number variation3nstd224human GRCh37 chr19: 52,272,131-52,588,718 , GRCh38.p12 chr19: 51,768,878-52,085,465 FPR2, ZNF432, 16 more genes
    nsv6625226copy number variation1nstd224human GRCh37 chr19: 52,272,350-52,588,718 , GRCh38.p12 chr19: 51,769,097-52,085,465 ZNF577, LOC100419835, 16 more genes
    nsv6625225copy number variation2nstd224human GRCh37 chr19: 52,272,131-52,617,369 , GRCh38.p12 chr19: 51,768,878-52,114,116 FPR3, ZNF615, 17 more genes
    nsv6625224copy number variation1nstd224human GRCh37 chr19: 52,272,131-52,578,347 , GRCh38.p12 chr19: 51,768,878-52,075,094 FPR3, ZNF613, 16 more genes
    nsv6625223copy number variation1nstd224human GRCh37 chr19: 52,263,927-52,617,369 , GRCh38.p12 chr19: 51,760,674-52,114,116 FPR3, ZNF613, 17 more genes
    nsv6625172copy number variation1nstd224human GRCh37 chr19: 52,272,321-52,617,369 , GRCh38.p12 chr19: 51,769,068-52,114,116 ZNF350, ZNF577, 17 more genes
    nsv6599109inversion1nstd223human GRCh38 chr19: 52,031,762-52,032,720 , GRCh37.p13 chr19: 52,535,015-52,535,973 ZNF432
    nsv6597318inversion1nstd223human GRCh38 chr19: 52,036,725-52,037,642 , GRCh37.p13 chr19: 52,539,978-52,540,895 ZNF432
    nsv6534608copy number variation1nstd223human GRCh38 chr19: 52,034,943-52,053,891 , GRCh37.p13 chr19: 52,538,196-52,557,144 ZNF841, ZNF432
    nsv6532466copy number variation1nstd223human GRCh38 chr19: 52,026,253-52,043,251 , GRCh37.p13 chr19: 52,529,506-52,546,504 ZNF614, ZNF432, 1 more genes
    nsv6531565copy number variation1nstd223human GRCh38 chr19: 51,768,552-52,114,483 , GRCh37.p13 chr19: 52,271,805-52,617,736 LOC100419835, ZNF615, 17 more genes
    nsv6517250copy number variation1nstd223human GRCh38 chr19: 52,034,619-52,035,040 , GRCh37.p13 chr19: 52,537,872-52,538,293 ZNF432
    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
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