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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6677277copy number variation1nstd229human GRCh38 chr2: 37,091,077-37,096,014 , GRCh37.p13 chr2: 37,318,220-37,323,157 GPATCH11
    nsv6671607copy number variation1nstd229human GRCh38 chr2: 37,051,305-37,094,915 , GRCh37.p13 chr2: 37,278,448-37,322,058 HEATR5B, GPATCH11
    nsv6661908copy number variation1nstd229human GRCh38 chr2: 37,004,076-37,144,447 , GRCh37.p13 chr2: 37,231,219-37,371,590 HEATR5B, GPATCH11, 1 more genes
    nsv6658671copy number variation1nstd229human GRCh38 chr2: 37,095,701-37,103,300 , GRCh37.p13 chr2: 37,322,844-37,330,443 EIF2AK2, GPATCH11
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628113copy number variation1nstd224human GRCh37 chr2: 37,227,797-37,327,244 , GRCh38.p12 chr2: 37,000,654-37,100,101 EIF2AK2, GPATCH11, 1 more genes
    nsv6549542inversion1nstd223human GRCh38 chr2: 32,866,974-37,651,961 , GRCh37.p13 chr2: 33,092,041-37,879,104 QPCT, TYW1P1, 55 more genes
    nsv6548859inversion1nstd223human GRCh38 chr2: 32,866,975-38,526,880 , GRCh37.p13 chr2: 33,092,042-38,754,022 ATP6V0E1P3, ARL14EPP1, 76 more genes
    nsv6548072inversion1nstd223human GRCh38 chr2: 32,866,995-42,468,982 , GRCh37.p13 chr2: 33,092,062-42,696,122 PKDCC, SRSF7, 127 more genes
    nsv6544899inversion1nstd223human GRCh38 chr2: 32,866,958-38,386,116 , GRCh37.p13 chr2: 33,092,025-38,613,258 ATP6V0E1P3, H2ACP2, 72 more genes
    nsv6544571inversion1nstd223human GRCh38 chr2: 32,867,025-38,327,253 , GRCh37.p13 chr2: 33,092,092-38,554,395 MIR548AD, LOC107985870, 72 more genes
    nsv6542757inversion1nstd223human GRCh38 chr2: 32,866,974-42,451,061 , GRCh37.p13 chr2: 33,092,041-42,678,201 RASGRP3, TTC39DP, 125 more genes
    nsv6540167inversion1nstd223human GRCh38 chr2: 32,866,952-40,818,398 , GRCh37.p13 chr2: 33,092,019-41,045,538 CEBPZOS, RNU6-1116P, 110 more genes
    nsv6539485inversion1nstd223human GRCh38 chr2: 32,866,964-42,766,565 , GRCh37.p13 chr2: 33,092,031-42,993,705 RN7SL602P, RNU6-851P, 132 more genes
    nsv6350616copy number variation1nstd223human GRCh38 chr2: 37,051,305-37,094,890 , GRCh37.p13 chr2: 37,278,448-37,322,033 GPATCH11, HEATR5B
    nsv6341850copy number variation1nstd223human GRCh38 chr2: 36,924,201-37,188,000 , GRCh37.p13 chr2: 37,151,344-37,415,143 EIF2AK2, STRN, 4 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313619copy number variation1nstd102humanPathogenic GRCh37 chr2: 29,899,368-42,441,440 , GRCh38.p12 chr2: 29,676,502-42,214,300 LOC107985870, SLC25A5P2, 161 more genes
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
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