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Items: 1 to 20 of 493

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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
    nsv7049114inversion1nstd229human GRCh38 chr2: 36,365,721-36,370,373 , GRCh37.p13 chr2: 36,592,864-36,597,516 CRIM1
    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
    nsv6677802copy number variation1nstd229human GRCh38 chr2: 36,539,057-36,544,346 , GRCh37.p13 chr2: 36,766,200-36,771,489 CRIM1
    nsv6676606copy number variation1nstd229human GRCh38 chr2: 36,511,261-36,671,347 , GRCh37.p13 chr2: 36,738,404-36,898,490 RACK1P2, FEZ2, 1 more genes
    nsv6675484copy number variation1nstd229human GRCh38 chr2: 36,517,354-36,529,672 , GRCh37.p13 chr2: 36,744,497-36,756,815 CRIM1
    nsv6673901copy number variation1nstd229human GRCh38 chr2: 36,360,001-36,369,400 , GRCh37.p13 chr2: 36,587,144-36,596,543 CRIM1
    nsv6671950copy number variation1nstd229human GRCh38 chr2: 36,414,783-36,414,946 , GRCh37.p13 chr2: 36,641,926-36,642,089 CRIM1
    nsv6671652copy number variation1nstd229human GRCh38 chr2: 36,480,532-36,482,377 , GRCh37.p13 chr2: 36,707,675-36,709,520 CRIM1
    nsv6671634copy number variation1nstd229human GRCh38 chr2: 36,356,980-36,357,015 , GRCh37.p13 chr2: 36,584,123-36,584,158 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
    nsv6669420copy number variation1nstd229human GRCh38 chr2: 36,487,601-36,492,600 , GRCh37.p13 chr2: 36,714,744-36,719,743 CRIM1
    nsv6669230copy number variation1nstd229human GRCh38 chr2: 36,371,024-36,372,490 , GRCh37.p13 chr2: 36,598,167-36,599,633 CRIM1
    nsv6665158copy number variation1nstd229human GRCh38 chr2: 36,368,240-36,371,138 , GRCh37.p13 chr2: 36,595,383-36,598,281 CRIM1
    nsv6665076copy number variation1nstd229human GRCh38 chr2: 36,367,655-36,367,714 , GRCh37.p13 chr2: 36,594,798-36,594,857 CRIM1
    nsv6665067copy number variation1nstd229human GRCh38 chr2: 36,362,181-36,362,744 , GRCh37.p13 chr2: 36,589,324-36,589,887 CRIM1
    nsv6664998copy number variation1nstd229human GRCh38 chr2: 36,454,687-36,458,539 , GRCh37.p13 chr2: 36,681,830-36,685,682 CRIM1
    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
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