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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050703inversion1nstd229human GRCh38 chr2: 36,312,082-36,602,069 , GRCh37.p13 chr2: 36,539,225-36,829,212 FEZ2, CRIM1, 1 more genes
    nsv7045302inversion1nstd229human GRCh38 chr2: 36,316,335-36,447,850 , GRCh37.p13 chr2: 36,543,478-36,674,993 CRIM1, CRIM1-DT
    nsv7041454inversion1nstd229human GRCh38 chr2: 36,315,115-36,455,084 , GRCh37.p13 chr2: 36,542,258-36,682,227 CRIM1-DT, CRIM1
    nsv6671185copy number variation1nstd229human GRCh38 chr2: 36,350,823-36,354,129 , GRCh37.p13 chr2: 36,577,966-36,581,272 CRIM1, CRIM1-DT
    nsv6670893copy number variation1nstd229human GRCh38 chr2: 36,221,503-36,395,459 , GRCh37.p13 chr2: 36,448,646-36,622,602 CRIM1, RPL21P36, 1 more genes
    nsv6663869copy number variation1nstd229human GRCh38 chr2: 34,666,849-36,488,261 , GRCh37.p13 chr2: 34,891,916-36,715,404 MIR548AD, LOC105374458, 12 more genes
    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
    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
    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
    nsv4728619copy number variation1nstd102humanUncertain significance GRCh37 chr2: 36,432,453-38,182,274 , GRCh38.p12 chr2: 36,205,310-37,955,131 CDC42EP3, NDUFAF7, 30 more genes
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