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Items: 1 to 20 of 277

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7058001inversion1nstd229human GRCh38 chr6: 47,441,459-48,144,831 , GRCh37.p13 chr6: 47,409,195-48,112,567 ADGRF2, RPL27AP7, 9 more genes
    nsv7047571inversion1nstd229human GRCh38 chr6: 47,471,816-49,526,857 , GRCh37.p13 chr6: 47,439,552-49,494,570 MMUT, RN7SKP116, 19 more genes
    nsv7044146inversion1nstd229human GRCh38 chr6: 47,635,253-48,108,329 , GRCh37.p13 chr6: 47,602,989-48,076,065 OPN5, LOC107986601, 6 more genes
    nsv6793683copy number variation1nstd229human GRCh38 chr6: 47,670,805-47,676,456 , GRCh37.p13 chr6: 47,638,541-47,644,192 ADGRF2
    nsv6793608copy number variation1nstd229human GRCh38 chr6: 47,663,802-47,663,834 , GRCh37.p13 chr6: 47,631,538-47,631,570 ADGRF2
    nsv6790650copy number variation1nstd229human GRCh38 chr6: 47,655,000-47,663,538 , GRCh37.p13 chr6: 47,622,736-47,631,274 ADGRF2
    nsv6788360copy number variation1nstd229human GRCh38 chr6: 47,656,513-47,656,567 , GRCh37.p13 chr6: 47,624,249-47,624,303 ADGRF2
    nsv6786217copy number variation1nstd229human GRCh38 chr6: 47,665,400-47,672,261 , GRCh37.p13 chr6: 47,633,136-47,639,997 ADGRF2
    nsv6784930copy number variation1nstd229human GRCh38 chr6: 47,650,639-47,659,654 , GRCh37.p13 chr6: 47,618,375-47,627,390 ADGRF2
    nsv6411763copy number variation1nstd223human GRCh38 chr6: 46,841,055-48,021,507 , GRCh37.p13 chr6: 46,808,792-47,989,243 RPL27AP7, LOC105375082, 18 more genes
    nsv6405939copy number variation1nstd223human GRCh38 chr6: 47,656,803-47,658,262 , GRCh37.p13 chr6: 47,624,539-47,625,998 ADGRF2
    nsv6402384copy number variation1nstd223human GRCh38 chr6: 47,650,636-47,659,654 , GRCh37.p13 chr6: 47,618,372-47,627,390 ADGRF2
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6291309copy number variation1nstd102humanUncertain significance GRCh37 chr6: 47,410,548-47,701,681 , GRCh38.p12 chr6: 47,442,812-47,733,945 CD2AP, RN7SKP116, 4 more genes
    nsv6245110mobile element insertion1nstd215human GRCh38 chr6: 47,663,802-47,663,802 , GRCh37.p13 chr6: 47,631,538-47,631,538 ADGRF2
    nsv6185957copy number variation1nstd214human GRCh38 chr6: 47,663,782-47,663,832 , GRCh37.p13 chr6: 47,631,518-47,631,568 ADGRF2
    nsv6179499copy number variation1nstd214human GRCh38 chr6: 47,663,783-47,663,832 , GRCh37.p13 chr6: 47,631,519-47,631,568 ADGRF2
    nsv6178927copy number variation1nstd214human GRCh38 chr6: 47,663,780-47,663,834 , GRCh37.p13 chr6: 47,631,516-47,631,570 ADGRF2
    nsv6175504copy number variation1nstd214human GRCh38 chr6: 47,663,780-47,663,832 , GRCh37.p13 chr6: 47,631,516-47,631,568 ADGRF2
    nsv6175499copy number variation1nstd214human GRCh38 chr6: 47,663,781-47,663,832 , GRCh37.p13 chr6: 47,631,517-47,631,568 ADGRF2
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