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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7138380insertion1nstd232human GRCh37.p13 chr2: 195,218,661-195,218,661 , GRCh38.p12 chr2: 194,353,937-194,353,937 LINC01821
    nsv6697182copy number variation1nstd229human GRCh38 chr2: 192,562,889-202,434,958 , GRCh37.p13 chr2: 193,427,615-203,299,681 RNU6-915P, SLC44A3P1, 150 more genes
    nsv6697093copy number variation1nstd229human GRCh38 chr2: 194,060,576-194,511,336 , GRCh37.p13 chr2: 194,925,300-195,376,060 LOC100419812, LINC01821, 3 more genes
    nsv6696780copy number variation1nstd229human GRCh38 chr2: 194,397,630-194,409,812 , GRCh37.p13 chr2: 195,262,354-195,274,536 LINC01821
    nsv6696526copy number variation1nstd229human GRCh38 chr2: 194,417,976-194,442,768 , GRCh37.p13 chr2: 195,282,700-195,307,492 LINC01821
    nsv6695527copy number variation1nstd229human GRCh38 chr2: 194,368,201-194,431,900 , GRCh37.p13 chr2: 195,232,925-195,296,624 LINC01821, LOC105373816
    nsv6694783copy number variation1nstd229human GRCh38 chr2: 194,383,372-194,383,487 , GRCh37.p13 chr2: 195,248,096-195,248,211 LOC105373816, LINC01821
    nsv6694188copy number variation1nstd229human GRCh38 chr2: 194,389,137-194,402,110 , GRCh37.p13 chr2: 195,253,861-195,266,834 LINC01821
    nsv6694125copy number variation1nstd229human GRCh38 chr2: 194,364,350-194,369,644 , GRCh37.p13 chr2: 195,229,074-195,234,368 LINC01821
    nsv6693289copy number variation1nstd229human GRCh38 chr2: 194,334,585-194,343,856 , GRCh37.p13 chr2: 195,199,309-195,208,580 LINC01821
    nsv6693054copy number variation1nstd229human GRCh38 chr2: 194,196,001-194,352,800 , GRCh37.p13 chr2: 195,060,725-195,217,524 LINC01821
    nsv6692885copy number variation1nstd229human GRCh38 chr2: 194,324,677-194,450,006 , GRCh37.p13 chr2: 195,189,401-195,314,730 LOC105373816, LINC01821
    nsv6692388copy number variation1nstd229human GRCh38 chr2: 194,343,537-194,343,693 , GRCh37.p13 chr2: 195,208,261-195,208,417 LINC01821
    nsv6688695copy number variation1nstd229human GRCh38 chr2: 194,349,101-194,355,200 , GRCh37.p13 chr2: 195,213,825-195,219,924 LINC01821
    nsv6688306copy number variation1nstd229human GRCh38 chr2: 194,350,146-194,378,385 , GRCh37.p13 chr2: 195,214,870-195,243,109 LOC105373816, LINC01821
    nsv6686214copy number variation1nstd229human GRCh38 chr2: 194,398,526-194,477,410 , GRCh37.p13 chr2: 195,263,250-195,342,134 LINC01821, LOC100419812
    nsv6686152copy number variation1nstd229human GRCh38 chr2: 194,378,444-194,386,777 , GRCh37.p13 chr2: 195,243,168-195,251,501 LINC01821, LOC105373816
    nsv6685533copy number variation1nstd229human GRCh38 chr2: 194,353,322-194,367,035 , GRCh37.p13 chr2: 195,218,046-195,231,759 LINC01821
    nsv6685255copy number variation1nstd229human GRCh38 chr2: 194,392,455-194,395,554 , GRCh37.p13 chr2: 195,257,179-195,260,278 LINC01821
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