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Items: 1 to 20 of 133

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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
    nsv7071936inversion1nstd229human GRCh38 chr19: 52,321,608-53,449,917 , GRCh37.p13 chr19: 52,824,861-53,953,171 ZNF528, ZNF321P, 54 more genes
    nsv7069393inversion1nstd229human GRCh38 chr19: 53,026,789-54,633,410 , GRCh37.p13 chr19: 53,530,042-54,528,887 MIR512-2, LILRB3, 145 more genes
    nsv7068840inversion1nstd229human GRCh38 chr19: 52,638,866-53,847,386 , GRCh37.p13 chr19: 53,142,119-54,350,640 MIR1283-2, MIR515-1, 115 more genes
    nsv7067028inversion1nstd229human GRCh38 chr19: 52,146,775-53,268,779 , GRCh37.p13 chr19: 52,650,028-53,772,032 ZNF528-AS1, ERVV-1, 47 more genes
    nsv7065131inversion1nstd229human GRCh38 chr19: 52,267,822-54,176,069 , GRCh37.p13 chr19: 52,771,075-54,528,887 ERVV-1, NDUFA3, 149 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
    nsv7059345inversion1nstd229human GRCh38 chr19: 52,208,319-53,617,958 , GRCh37.p13 chr19: 52,711,572-54,121,212 ZNF677, ZNF611, 71 more genes
    nsv7013704copy number variation1nstd229human GRCh38 chr19: 52,613,341-53,295,254 , GRCh37.p13 chr19: 53,116,594-53,798,507 ZNF415, ZNF347, 28 more genes
    nsv7013108copy number variation1nstd229human GRCh38 chr19: 53,254,604-53,447,937 , GRCh37.p13 chr19: 53,757,857-53,951,190 ZNF845, ZNF765, 16 more genes
    nsv7006834copy number variation1nstd229human GRCh38 chr19: 53,157,830-53,636,507 , GRCh37.p13 chr19: 53,661,083-54,139,761 ZNF818P, VN1R103P, 32 more genes
    nsv7004963copy number variation1nstd229human GRCh38 chr19: 53,257,817-53,264,330 , GRCh37.p13 chr19: 53,761,070-53,767,583 VN1R2, VN1R4
    nsv7001942copy number variation1nstd229human GRCh38 chr19: 53,269,601-53,270,700 , GRCh37.p13 chr19: 53,772,854-53,773,953 VN1R4
    nsv6998409copy number variation1nstd229human GRCh38 chr19: 53,266,553-53,266,720 , GRCh37.p13 chr19: 53,769,806-53,769,973 VN1R4
    nsv6637832copy number variation1nstd102humanUncertain significance GRCh37 chr19: 53,723,679-53,787,396 , GRCh38.p12 chr19: 53,220,426-53,284,143 VN1R4, FAM90A27P, 3 more genes
    nsv6625280copy number variation1nstd224human GRCh37 chr19: 53,647,478-53,932,295 , GRCh38.p12 chr19: 53,144,225-53,429,042 VN1R4, FAM90A27P, 19 more genes
    nsv6625185copy number variation1nstd224human GRCh37 chr19: 53,770,879-53,803,810 , GRCh38.p12 chr19: 53,267,626-53,300,557 VN1R4, FAM90A27P, 3 more genes
    nsv6599385inversion1nstd223human GRCh38 chr19: 52,690,198-53,366,220 , GRCh37.p13 chr19: 53,193,451-53,869,473 NDUFV2P1, ZNF28, 33 more genes
    nsv6598106inversion1nstd223human GRCh38 chr19: 52,978,469-53,338,700 , GRCh37.p13 chr19: 53,481,722-53,841,953 ERVV-1, ZNF160, 19 more genes
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