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Items: 1 to 20 of 1278

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148242copy number variation1nstd102humanPathogenic GRCh38 chr15: 20,966,971-25,963,714 , GRCh37.p13 chr15: 21,172,300-26,208,861 LOC101269108, LOC107983983, 227 more genes
    nsv7148087copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,744,149-23,246,340 , GRCh38.p12 chr15: 22,626,756-23,128,919 ELMO2P1, LOC729900, 12 more genes
    nsv7145448copy number variation1nstd232human GRCh37.p13 chr15: 22,933,654-22,933,743 , GRCh38.p12 chr15: 22,939,325-22,939,414 , GRCh38.p12 chr15|NT_187603.1: 36,354-36,443 CYFIP1
    nsv7137212copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-23,195,725 , GRCh38.p12 chr15: 22,677,371-23,102,647 LOC100133165, PDCD6IPP1, 10 more genes
    nsv7137131copy number variation2nstd102humanPathogenic GRCh37 chr15: 22,833,525-23,412,276 , GRCh38.p12 chr15: 22,460,820-23,039,543 PDCD6IPP1, LOC100419579, 17 more genes
    nsv7137111copy number variation1nstd102humanUncertain significance GRCh37 chr15: 22,739,723-23,259,294 , GRCh38.p12 chr15: 22,613,802-23,133,345 GOLGA8IP, CYFIP1, 13 more genes
    nsv7137110copy number variation1nstd102humanUncertain significance GRCh37 chr15: 22,835,916-23,264,190 , GRCh38.p12 chr15: 22,608,906-23,037,152 LOC100132817, NIPA2, 12 more genes
    nsv7137107copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,499-23,577,516 , GRCh38.p12 chr15: 22,358,243-23,039,569 TUBGCP5, GOLGA8IP, 22 more genes
    nsv7098946copy number variation1nstd102humanUncertain significance GRCh38 chr15: 22,787,668-23,051,531 , GRCh37.p13 chr15: 22,821,537-23,085,400 CYFIP1, NIPA2, 2 more genes
    nsv7098937copy number variation1nstd102humanUncertain significance GRCh38 chr15: 22,781,888-23,030,923 , GRCh37.p13 chr15: 22,842,145-23,091,180 CYFIP1, NIPA2, 2 more genes
    nsv7098915copy number variation1nstd102humanUncertain significance GRCh38 chr15: 22,787,849-23,051,049 , GRCh37.p13 chr15: 22,822,019-23,085,219 NIPA2, NIPA1, 2 more genes
    nsv7098876copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,070,540-23,262,343 , GRCh38.p12 chr15: 22,610,753-23,226,874 RN7SL106P, GOLGA6L1, 20 more genes
    nsv7098836copy number variation1nstd102humanPathogenic GRCh38 chr15: 22,698,177-23,380,983 , GRCh37.p13 chr15: 22,646,194-23,174,919 TUBGCP5, GOLGA8S, 25 more genes
    nsv7093398copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,525-23,262,343 , GRCh38.p12 chr15: 22,610,753-23,039,543 LOC101927846, NIPA1, 11 more genes
    nsv7093386copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,525-23,264,190 , GRCh38.p12 chr15: 22,608,906-23,039,543 CYFIP1, LOC101927846, 12 more genes
    nsv7065496inversion1nstd229human GRCh38 chr15: 20,672,644-28,900,286 , GRCh37.p13 chr15: 20,877,973-29,145,432 SNURF, LOC101060118, 290 more genes
    nsv7064061inversion1nstd229human GRCh38 chr15: 22,875,659-22,875,743 , GRCh37.p13 chr15: 22,997,325-22,997,409 CYFIP1
    nsv7062890inversion1nstd229human GRCh38 chr15: 22,884,838-22,884,969 , GRCh37.p13 chr15: 22,988,099-22,988,230 CYFIP1
    nsv6976531copy number variation1nstd229human GRCh38 chr15: 22,875,473-22,875,540 , GRCh37.p13 chr15: 22,997,528-22,997,595 CYFIP1
    nsv6974463copy number variation1nstd229human GRCh38 chr15: 22,962,562-22,967,046 , GRCh37.p13 chr15: 22,906,022-22,910,506 CYFIP1
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