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Items: 1 to 20 of 480

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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
    nsv7141031insertion1nstd232human GRCh37.p13 chr2: 213,990,905-213,990,905 , GRCh38.p12 chr2: 213,126,181-213,126,181 IKZF2
    nsv7040916inversion1nstd229human GRCh38 chr2: 213,064,207-213,064,244 , GRCh37.p13 chr2: 213,928,931-213,928,968 IKZF2
    nsv6696966copy number variation1nstd229human GRCh38 chr2: 212,983,822-213,359,890 , GRCh37.p13 chr2: 213,848,546-214,224,614 SPAG16-DT, LINC01953, 5 more genes
    nsv6696003copy number variation1nstd229human GRCh38 chr2: 213,060,641-213,106,628 , GRCh37.p13 chr2: 213,925,365-213,971,352 IKZF2
    nsv6695407copy number variation1nstd229human GRCh38 chr2: 213,030,447-213,044,083 , GRCh37.p13 chr2: 213,895,171-213,908,807 IKZF2
    nsv6691566copy number variation1nstd229human GRCh38 chr2: 213,102,659-213,120,291 , GRCh37.p13 chr2: 213,967,383-213,985,015 IKZF2
    nsv6690520copy number variation1nstd229human GRCh38 chr2: 213,065,850-213,067,977 , GRCh37.p13 chr2: 213,930,574-213,932,701 IKZF2
    nsv6689720copy number variation1nstd229human GRCh38 chr2: 213,155,269-213,178,462 , GRCh37.p13 chr2: 214,019,993-214,043,186 LOC105373864, IKZF2, 1 more genes
    nsv6689674copy number variation1nstd229human GRCh38 chr2: 213,132,280-213,135,422 , GRCh37.p13 chr2: 213,997,004-214,000,146 IKZF2
    nsv6688434copy number variation1nstd229human GRCh38 chr2: 213,147,991-213,462,824 , GRCh37.p13 chr2: 214,012,715-214,327,548 SPAG16-DT, SPAG16, 4 more genes
    nsv6687932copy number variation1nstd229human GRCh38 chr2: 213,115,213-213,121,582 , GRCh37.p13 chr2: 213,979,937-213,986,306 IKZF2
    nsv6687716copy number variation1nstd229human GRCh38 chr2: 213,086,700-213,090,162 , GRCh37.p13 chr2: 213,951,424-213,954,886 IKZF2
    nsv6686783copy number variation1nstd229human GRCh38 chr2: 213,076,663-213,083,943 , GRCh37.p13 chr2: 213,941,387-213,948,667 IKZF2
    nsv6685964copy number variation1nstd229human GRCh38 chr2: 213,061,204-213,070,442 , GRCh37.p13 chr2: 213,925,928-213,935,166 IKZF2
    nsv6685560copy number variation1nstd229human GRCh38 chr2: 213,064,149-213,064,264 , GRCh37.p13 chr2: 213,928,873-213,928,988 IKZF2
    nsv6684691copy number variation1nstd229human GRCh38 chr2: 212,579,301-213,328,500 , GRCh37.p13 chr2: 213,444,025-214,193,224 IKZF2, MIR4776-1, 10 more genes
    nsv6684104copy number variation1nstd229human GRCh38 chr2: 213,102,984-213,109,180 , GRCh37.p13 chr2: 213,967,708-213,973,904 IKZF2
    nsv6683784copy number variation1nstd229human GRCh38 chr2: 213,126,672-213,132,152 , GRCh37.p13 chr2: 213,991,396-213,996,876 IKZF2
    nsv6683155copy number variation1nstd229human GRCh38 chr2: 213,124,947-213,141,551 , GRCh37.p13 chr2: 213,989,671-214,006,275 IKZF2
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