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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4675660copy number variation1nstd102humanUncertain significance GRCh37 chr15: 69,681,832-69,906,547 , GRCh38.p12 chr15: 69,389,493-69,614,208 PAQR5, KIF23-AS1, 6 more genes
    nsv4625771copy number variation1nstd183human GRCh37 chr15: 69,706,456-69,706,743 , GRCh38.p12 chr15: 69,414,117-69,414,404 KIF23-AS1, KIF23
    nsv4510395mobile element insertion1nstd166human GRCh37.p13 chr15: 69,699,948-69,699,948 , GRCh38.p12 chr15: 69,407,609-69,407,609 KIF23-AS1, PAQR5
    nsv4456268copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,369,118-70,481,307 , GRCh38.p12 chr15: 67,076,780-70,188,968 ANP32A-IT1, CARS1P1, 48 more genes
    nsv4338323sequence alteration1nstd166human GRCh37.p13 chr15: 69,446,476-72,211,091 , GRCh38.p12 chr15: 69,154,137-71,918,750 , MYO9A, 45 more genes
    nsv4247414copy number variation1nstd166human GRCh37.p13 chr15: 69,697,849-69,698,109 , GRCh38.p12 chr15: 69,405,510-69,405,770 KIF23-AS1, PAQR5
    nsv4235184copy number variation1nstd166human GRCh37.p13 chr15: 69,695,992-69,696,054 , GRCh38.p12 chr15: 69,403,653-69,403,715 KIF23-AS1, PAQR5
    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
    nsv3920633copy number variation1nstd102humanPathogenic GRCh38 chr15: 68,830,574-73,823,337 , NCBI36 chr15: 66,909,967-71,902,731 , GRCh37 chr15: 69,122,913-74,115,678 NEO1, LOC390600, 95 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
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 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
    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
    nsv3905308copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 59,297,293-102,480,888 , GRCh38.p12 chr15: 59,005,094-101,940,685 ACAN, ALDH1A3, 861 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
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