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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939106copy number variation1nstd209human GRCh38 chr15: 38,008,106-40,186,655 , GRCh37.p13 chr15: 38,300,307-40,478,856 , LOC105370784, 36 more genes
    nsv5513748copy number variation1nstd206human GRCh38 chr15: 39,780,246-39,791,240 , GRCh37.p13 chr15: 40,072,447-40,083,441 LOC105370941, FSIP1
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5005284copy number variation1nstd200human GRCh38 chr15: 39,356,836-39,812,806 , GRCh37.p13 chr15: 39,649,037-40,105,007 LOC105370941, LOC105370785, 5 more genes
    nsv4436396complex substitution1nstd102humanPathogenic GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083 ACTC1, BUB1B, 150 more genes
    nsv4245044copy number variation1nstd166human GRCh37.p13 chr15: 39,649,067-40,105,007 , GRCh38.p12 chr15: 39,356,866-39,812,806 THBS1, GPR176, 5 more genes
    nsv3923477copy number variation1nstd102humanUncertain significance NCBI36 chr15: 37,790,428-38,374,084 , GRCh37 chr15: 40,003,136-40,586,792 , GRCh38 chr15: 39,710,935-40,294,591 BMF, MTND5P37, 17 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
    nsv3915967copy number variation1nstd102humanPathogenic GRCh38 chr15: 32,635,803-40,233,825 , GRCh37 chr15: 32,928,004-40,526,026 , NCBI36 chr15: 30,715,296-38,313,318 ANP32AP1, FMN1, 112 more genes
    nsv3915210copy number variation1nstd102humanUncertain significance NCBI36 chr15: 28,207,117-100,338,915 , GRCh37.p13 chr15: 30,419,825-102,521,392 , GRCh38.p12 chr15: 30,127,622-101,981,189 RPL21P113, LOC112268152, 1428 more genes
    nsv3913581copy number variation1nstd102humanPathogenic NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189 MIR4513, LOC727751, 1754 more genes
    nsv3911945copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,203,424-100,338,915 , GRCh37.p13 chr15: 22,652,060-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 HDDC3, TRK-CTT16-1, 1622 more genes
    nsv3905138copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413 FES, OR4H6BP, 1738 more genes
    nsv3904086copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959 TMEM202, SNORD115-28, 1747 more genes
    nsv3903574copy number variation1nstd102humanPathogenic GRCh37 chr15: 38,170,429-40,775,075 , GRCh38.p12 chr15: 37,878,228-40,482,876 CHST14, LOC105370783, 49 more genes
    nsv3900281copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337 MYZAP, JMJD7, 1750 more genes
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