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Items: 1 to 20 of 465

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148172copy number variation1nstd102humanPathogenic GRCh38 chr15: 50,923,067-50,925,830 , GRCh37.p13 chr15: 51,215,264-51,218,027 AP4E1
    nsv7148115copy number variation1nstd102humanUncertain significance GRCh37 chr15: 49,775,348-51,221,365 , GRCh38.p12 chr15: 49,483,151-50,929,168 RNA5SP395, AHCYP7, 24 more genes
    nsv7094718copy number variation1nstd102humanUncertain significance GRCh37 chr15: 51,200,976-51,226,914 , GRCh38.p12 chr15: 50,908,779-50,934,717 AP4E1
    nsv7094385copy number variation2nstd102humanPathogenic GRCh37 chr15: 50,999,997-54,025,330 , GRCh38.p12 chr15: 50,707,800-53,733,133 LOC105370826, MIR7973-2, 48 more genes
    nsv7094384copy number variation1nstd102humanUncertain significance GRCh37 chr15: 50,731,271-54,025,330 , GRCh38.p12 chr15: 50,439,074-53,733,133 LOC105370823, TMOD3, 54 more genes
    nsv7073737inversion1nstd229human GRCh38 chr15: 50,073,562-51,225,515 , GRCh37.p13 chr15: 50,365,759-51,517,712 DCAF13P3, TRPM7, 21 more genes
    nsv7069161inversion1nstd229human GRCh38 chr15: 50,963,483-51,066,914 , GRCh37.p13 chr15: 51,255,680-51,359,111 TNFAIP8L3, AP4E1, 1 more genes
    nsv7067502inversion1nstd229human GRCh38 chr15: 48,513,881-51,354,383 , GRCh37.p13 chr15: 48,806,078-51,646,580 NDUFAF4P1, MIR4713, 49 more genes
    nsv6977566copy number variation1nstd229human GRCh38 chr15: 50,475,532-50,938,408 , GRCh37.p13 chr15: 50,767,729-51,230,605 TRPM7, USP8, 5 more genes
    nsv6977309copy number variation1nstd229human GRCh38 chr15: 50,961,314-50,961,402 , GRCh37.p13 chr15: 51,253,511-51,253,599 AP4E1
    nsv6975491copy number variation1nstd229human GRCh38 chr15: 50,978,601-50,982,500 , GRCh37.p13 chr15: 51,270,798-51,274,697 AP4E1
    nsv6975278copy number variation1nstd229human GRCh38 chr15: 50,962,907-51,163,162 , GRCh37.p13 chr15: 51,255,104-51,455,359 TNFAIP8L3, AP4E1, 1 more genes
    nsv6974596copy number variation1nstd229human GRCh38 chr15: 50,953,731-50,953,823 , GRCh37.p13 chr15: 51,245,928-51,246,020 AP4E1
    nsv6973654copy number variation1nstd229human GRCh38 chr15: 50,975,441-50,976,825 , GRCh37.p13 chr15: 51,267,638-51,269,022 AP4E1
    nsv6970454copy number variation1nstd229human GRCh38 chr15: 50,905,317-50,917,830 , GRCh37.p13 chr15: 51,197,514-51,210,027 AP4E1
    nsv6969068copy number variation1nstd229human GRCh38 chr15: 50,535,273-50,928,825 , GRCh37.p13 chr15: 50,827,470-51,221,022 TRPM7, RPL32P30, 4 more genes
    nsv6965496copy number variation1nstd229human GRCh38 chr15: 50,893,895-51,071,958 , GRCh37.p13 chr15: 51,186,092-51,364,155 DCAF13P3, TNFAIP8L3, 2 more genes
    nsv6965193copy number variation1nstd229human GRCh38 chr15: 50,910,587-50,921,245 , GRCh37.p13 chr15: 51,202,784-51,213,442 AP4E1
    nsv6964209copy number variation1nstd229human GRCh38 chr15: 50,876,762-50,996,445 , GRCh37.p13 chr15: 51,168,959-51,288,642 DCAF13P3, AP4E1
    nsv6963920copy number variation1nstd229human GRCh38 chr15: 50,582,205-51,473,799 , GRCh37.p13 chr15: 50,874,402-51,765,996 RN7SL354P, DCAF13P3, 13 more genes
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