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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099246copy number variation1nstd231human GRCh38.p12 chr1: 170,327,769-171,350,588 , GRCh37 chr1: 170,296,910-171,319,727 FMO1, FMO2, 16 more genes
    nsv6644575copy number variation1nstd229human GRCh38 chr1: 171,285,897-171,289,995 , GRCh37.p13 chr1: 171,255,036-171,259,134 FMO1
    nsv6644569copy number variation1nstd229human GRCh38 chr1: 171,089,340-171,371,617 , GRCh37.p13 chr1: 171,058,481-171,340,756 FMO3, MIR1295A, 9 more genes
    nsv6644459copy number variation1nstd229human GRCh38 chr1: 171,285,638-171,288,808 , GRCh37.p13 chr1: 171,254,777-171,257,947 FMO1
    nsv6644458copy number variation1nstd229human GRCh38 chr1: 171,284,322-171,285,896 , GRCh37.p13 chr1: 171,253,461-171,255,035 FMO1
    nsv6644453copy number variation1nstd229human GRCh38 chr1: 171,117,583-171,372,251 , GRCh37.p13 chr1: 171,086,723-171,341,390 FMO2, SRP14P4, 7 more genes
    nsv6644083copy number variation1nstd229human GRCh38 chr1: 171,262,101-171,267,200 , GRCh37.p13 chr1: 171,231,240-171,236,339 FMO1
    nsv6644082copy number variation1nstd229human GRCh38 chr1: 171,244,740-171,347,845 , GRCh37.p13 chr1: 171,213,879-171,316,984 SRP14P4, HMGB1P11, 4 more genes
    nsv6636536copy number variation1nstd102humanUncertain significance GRCh37 chr1: 171,186,446-171,907,499 , GRCh38.p12 chr1: 171,217,307-171,938,359 METTL13, MYOC, 22 more genes
    nsv6625809copy number variation1nstd224human GRCh37 chr1: 171,019,772-171,350,357 , GRCh38.p12 chr1: 171,050,631-171,381,218 FMO1, FMO4, 11 more genes
    nsv6332992copy number variation1nstd223human GRCh38 chr1: 171,281,171-171,281,777 , GRCh37.p13 chr1: 171,250,310-171,250,916 FMO1
    nsv6332322copy number variation1nstd223human GRCh38 chr1: 171,275,858-171,276,594 , GRCh37.p13 chr1: 171,244,997-171,245,733 FMO1
    nsv6323855copy number variation1nstd223human GRCh38 chr1: 171,264,862-171,265,330 , GRCh37.p13 chr1: 171,234,001-171,234,469 FMO1
    nsv6316096copy number variation1nstd223human GRCh38 chr1: 171,285,638-171,288,806 , GRCh37.p13 chr1: 171,254,777-171,257,945 FMO1
    nsv6313719copy number variation1nstd102humanPathogenic GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192 LOC100420658, LOC105371610, 167 more genes
    nsv6313602copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,391,422-171,843,613 , GRCh38.p12 chr1: 167,422,185-171,874,473 DCAF6, SELE, 101 more genes
    nsv6297399copy number variation1nstd186human GRCh37 chr1: 171,234,001-171,234,216 , GRCh38.p12 chr1: 171,264,862-171,265,077 FMO1
    nsv6245603mobile element insertion1nstd215human GRCh38 chr1: 171,284,196-171,284,196 , GRCh37.p13 chr1: 171,253,335-171,253,335 FMO1
    nsv6133940copy number variation1nstd213human GRCh37 chr1: 170,740,000-173,330,001 , GRCh38.p12 chr1: 170,770,859-173,360,862 TNFSF4, VAMP4, 50 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
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