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Items: 1 to 20 of 174

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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
    nsv6644683copy number variation1nstd229human GRCh38 chr1: 171,342,279-171,350,499 , GRCh37.p13 chr1: 171,311,418-171,319,638 SRP14P4, FMO4
    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
    nsv6644460copy number variation1nstd229human GRCh38 chr1: 171,325,094-171,410,415 , GRCh37.p13 chr1: 171,294,233-171,379,554 SRP14P4, GM2AP2, 2 more genes
    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
    nsv6644088copy number variation1nstd229human GRCh38 chr1: 171,338,914-171,356,832 , GRCh37.p13 chr1: 171,308,053-171,325,971 SRP14P4, TOP1P1, 1 more genes
    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
    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
    nsv6290403copy number variation1nstd102humanLikely benign GRCh37 chr1: 171,294,383-171,371,123 , GRCh38.p12 chr1: 171,325,244-171,401,984 FMO4, TOP1P1, 2 more genes
    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
    nsv6133569copy number variation1nstd213human GRCh37 chr1: 171,300,000-171,410,001 , GRCh38.p12 chr1: 171,330,861-171,440,862 FMO4, TOP1P1, 3 more genes
    nsv6133568copy number variation1nstd213human GRCh37 chr1: 170,840,000-171,410,001 , GRCh38.p12 chr1: 170,870,859-171,440,862 FMO3, TOP1P1, 13 more genes
    nsv6133567copy number variation1nstd213human GRCh37 chr1: 170,760,000-174,730,001 , GRCh38.p12 chr1: 170,790,859-174,760,863 FASLG, SERPINC1, 87 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4898022copy number variation1nstd200human GRCh38 chr1: 171,325,089-171,410,428 , GRCh37.p13 chr1: 171,294,228-171,379,567 GM2AP2, SRP14P4, 2 more genes
    nsv4784664copy number variation1nstd200human GRCh37 chr1: 171,294,228-171,379,567 , GRCh38.p12 chr1: 171,325,089-171,410,428 GM2AP2, TOP1P1, 2 more genes
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