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Items: 1 to 20 of 302

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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
    nsv7049459inversion1nstd229human GRCh38 chr2: 199,624,566-202,238,851 , GRCh37.p13 chr2: 200,489,289-203,103,574 LOC105373833, NDUFB3, 76 more genes
    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
    nsv6696268copy number variation1nstd229human GRCh38 chr2: 201,343,356-201,349,481 , GRCh37.p13 chr2: 202,208,079-202,214,204 FLACC1
    nsv6692949copy number variation1nstd229human GRCh38 chr2: 201,343,401-201,349,500 , GRCh37.p13 chr2: 202,208,124-202,214,223 FLACC1
    nsv6692528copy number variation1nstd229human GRCh38 chr2: 201,300,015-201,303,399 , GRCh37.p13 chr2: 202,164,738-202,168,122 FLACC1
    nsv6691459copy number variation1nstd229human GRCh38 chr2: 201,232,019-201,287,476 , GRCh37.p13 chr2: 202,096,742-202,152,199 FLACC1, CASP8
    nsv6690493copy number variation1nstd229human GRCh38 chr2: 201,259,135-201,290,143 , GRCh37.p13 chr2: 202,123,858-202,154,866 FLACC1, CASP8
    nsv6688798copy number variation1nstd229human GRCh38 chr2: 201,336,308-201,345,056 , GRCh37.p13 chr2: 202,201,031-202,209,779 FLACC1
    nsv6688178copy number variation1nstd229human GRCh38 chr2: 201,359,101-201,391,200 , GRCh37.p13 chr2: 202,223,824-202,255,923 FLACC1, TRAK2
    nsv6683936copy number variation1nstd229human GRCh38 chr2: 201,211,425-201,312,149 , GRCh37.p13 chr2: 202,076,148-202,176,872 CASP10, MTND4P23, 4 more genes
    nsv6683056copy number variation1nstd229human GRCh38 chr2: 201,301,884-201,312,446 , GRCh37.p13 chr2: 202,166,607-202,177,169 FLACC1
    nsv6679260copy number variation1nstd229human GRCh38 chr2: 201,342,198-201,398,770 , GRCh37.p13 chr2: 202,206,921-202,263,493 FLACC1, TRAK2
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 LOC100421409, LOC100507443, 310 more genes
    nsv6353176copy number variation1nstd223human GRCh38 chr2: 201,347,631-201,349,539 , GRCh37.p13 chr2: 202,212,354-202,214,262 FLACC1
    nsv6345546copy number variation1nstd223human GRCh38 chr2: 201,343,356-201,349,477 , GRCh37.p13 chr2: 202,208,079-202,214,200 FLACC1
    nsv6343711copy number variation1nstd223human GRCh38 chr2: 201,336,308-201,345,054 , GRCh37.p13 chr2: 202,201,031-202,209,777 FLACC1
    nsv6339815copy number variation1nstd223human GRCh38 chr2: 201,293,544-201,303,077 , GRCh37.p13 chr2: 202,158,267-202,167,800 FLACC1
    nsv6315398copy number variation1nstd102humanPathogenic GRCh37 chr2: 185,697,659-213,002,074 , GRCh38.p12 chr2: 184,832,932-212,137,349 LOC107985785, MYO1B, 381 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
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