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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv6686323copy number variation1nstd229human GRCh38 chr2: 230,884,132-230,891,984 , GRCh37.p13 chr2: 231,748,847-231,756,699 GCSIR
    nsv6684971copy number variation1nstd229human GRCh38 chr2: 230,901,301-230,907,100 , GRCh37.p13 chr2: 231,766,016-231,771,815 GPR55, GCSIR
    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
    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
    nsv6299973copy number variation1nstd186human GRCh37 chr2: 231,762,589-231,764,437 , GRCh38.p12 chr2: 230,897,874-230,899,722 GCSIR
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5440339copy number variation1nstd206human GRCh38 chr2: 230,897,874-230,899,722 , GRCh37.p13 chr2: 231,762,589-231,764,437 GCSIR
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4679888copy number variation1nstd189human GRCh37.p13 chr2: 231,366,319-232,108,260 , GRCh38.p12 chr2: 230,501,604-231,243,547 HTR2B, PSMD1, 21 more genes
    nsv4673913copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,814,690-242,783,384 , GRCh38.p12 chr2: 229,949,974-241,841,232 MIR2467, D2HGDH, 270 more genes
    nsv4435891copy number variation1nstd102humanPathogenic GRCh37 chr2: 210,779,657-239,879,183 , GRCh38.p12 chr2: 209,914,933-238,957,487 XRCC5, LINC01173, 494 more genes
    nsv3924332copy number variation1nstd102humanPathogenic NCBI36 chr2: 230,011,029-233,894,271 , GRCh37.p13 chr2: 230,302,785-234,229,532 , GRCh38.p12 chr2: 229,438,069-233,320,886 EIF4E2, LOC107985996, 100 more genes
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