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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141979insertion1nstd232human GRCh37.p13 chr2: 231,797,873-231,797,873 , GRCh38.p12 chr2: 230,933,158-230,933,158 GPR55
    nsv7054895inversion1nstd229human GRCh38 chr2: 229,787,965-232,576,060 , GRCh37.p13 chr2: 230,652,681-233,440,770 GPR55, RN7SL834P, 80 more genes
    nsv7039246inversion1nstd229human GRCh38 chr2: 230,817,971-230,981,097 , GRCh37.p13 chr2: 231,682,686-231,845,812 GPR55, COX20P2, 3 more genes
    nsv6697384copy number variation1nstd229human GRCh38 chr2: 230,903,964-230,908,077 , GRCh37.p13 chr2: 231,768,679-231,772,792 GPR55, GCSIR
    nsv6695687copy number variation1nstd229human GRCh38 chr2: 230,957,515-230,957,598 , GRCh37.p13 chr2: 231,822,230-231,822,313 COX20P2, GPR55
    nsv6693043copy number variation1nstd229human GRCh38 chr2: 230,829,401-231,058,500 , GRCh37.p13 chr2: 231,694,116-231,923,214 C2orf72, SPATA3, 7 more genes
    nsv6689136copy number variation1nstd229human GRCh38 chr2: 230,927,846-230,931,831 , GRCh37.p13 chr2: 231,792,561-231,796,546 GPR55
    nsv6688337copy number variation1nstd229human GRCh38 chr2: 230,945,253-230,945,441 , GRCh37.p13 chr2: 231,809,968-231,810,156 GPR55
    nsv6684971copy number variation1nstd229human GRCh38 chr2: 230,901,301-230,907,100 , GRCh37.p13 chr2: 231,766,016-231,771,815 GPR55, GCSIR
    nsv6682834copy number variation1nstd229human GRCh38 chr2: 230,958,806-230,960,734 , GRCh37.p13 chr2: 231,823,521-231,825,449 GPR55
    nsv6678540copy number variation1nstd229human GRCh38 chr2: 230,799,348-230,905,503 , GRCh37.p13 chr2: 231,664,063-231,770,218 CAB39, GCSIR, 2 more genes
    nsv6678243copy number variation1nstd229human GRCh38 chr2: 230,944,881-230,954,371 , GRCh37.p13 chr2: 231,809,596-231,819,086 GPR55
    nsv6678209copy number variation1nstd229human GRCh38 chr2: 230,950,772-230,951,267 , GRCh37.p13 chr2: 231,815,487-231,815,982 GPR55
    nsv6345727copy number variation1nstd223human GRCh38 chr2: 230,944,881-230,954,372 , GRCh37.p13 chr2: 231,809,596-231,819,087 GPR55
    nsv6337886copy number variation1nstd223human GRCh38 chr2: 230,949,578-230,950,024 , GRCh37.p13 chr2: 231,814,293-231,814,739 GPR55
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313761copy number variation1nstd102humanPathogenic GRCh37 chr2: 229,968,217-231,883,182 , GRCh38.p12 chr2: 229,103,501-231,018,467 SLC16A14, BANF1P3, 35 more genes
    nsv6313683copy number variation1nstd102humanPathogenic GRCh37 chr2: 228,807,574-235,475,892 , GRCh38.p12 chr2: 227,942,858-234,567,248 RNU7-9P, SCARNA5, 143 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 LOC105373947, RN7SL764P, 357 more genes
    nsv6311650copy number variation2nstd102humanUncertain significance GRCh37 chr2: 231,033,840-234,978,657 , GRCh38.p12 chr2: 230,169,124-234,070,013 SP110, LINC00471, 112 more genes
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