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Items: 1 to 20 of 44149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4805429copy number variation1nstd200human GRCh37 chr5: 45,120,233-46,135,433 , GRCh38.p12 chr5: 45,120,131-46,135,331 HCN1
    nsv4904177copy number variation1nstd200human GRCh38 chr1: 194,442,973-195,316,340 , GRCh37.p13 chr1: 194,412,103-195,285,470 RNU6-983P
    nsv4781351copy number variation1nstd200human GRCh37 chr1: 194,412,103-195,285,470 , GRCh38.p12 chr1: 194,442,973-195,316,340 RNU6-983P
    nsv4934787copy number variation1nstd200human GRCh38 chr6: 60,784,620-61,407,067 , GRCh37.p13 chr6: 57,752,367-58,087,660 RBBP4P3
    nsv4905122copy number variation1nstd200human GRCh38 chrX: 4,112,900-4,716,407 , GRCh37.p13 chrX: 4,030,941-4,634,448 LOC101928201
    nsv4909261copy number variation1nstd200human GRCh38 chrX: 148,851,332-149,418,082 , GRCh37.p13 chrX: 147,932,861-148,499,613 , GRCh37.p13 chrX|NW_004070890.2: 4,375,729-4,942,480 AFF2
    nsv4782430copy number variation1nstd200human GRCh37 chrX: 147,932,861-148,499,613 , GRCh38.p12 chrX: 148,851,332-149,418,082 AFF2
    nsv4925697copy number variation1nstd200human GRCh38 chr4: 62,719,218-63,269,298 , GRCh37.p13 chr4: 63,584,936-64,135,016 EXOC5P1
    nsv4905588copy number variation1nstd200human GRCh38 chrX: 66,714,274-67,258,717 , GRCh37.p13 chrX: 65,934,116-66,478,559 LOC105373240
    nsv4782079copy number variation1nstd200human GRCh37 chrX: 65,934,116-66,478,558 , GRCh38.p12 chrX: 66,714,274-67,258,716 LOC105373240
    nsv4909218copy number variation1nstd200human GRCh38 chrX: 144,218,751-144,760,932 , GRCh37.p13 chrX|NW_004070890.2: 1-285,326 , GRCh37.p13 chrX: 143,301,857-143,842,453 RRM2P4
    nsv4782404copy number variation1nstd200human GRCh37 chrX: 143,301,857-143,842,453 , GRCh38.p12 chrX: 144,218,751-144,760,932 RRM2P4
    nsv4905745copy number variation1nstd200human GRCh38 chrX: 90,515,271-91,053,560 , GRCh37.p13 chrX: 89,770,270-90,308,559 RNU6-555P
    nsv4772444copy number variation1nstd200human GRCh37 chrX: 2,026,196-2,362,015 , GRCh38.p12 chrX: 1,907,303-2,443,974 DHRSX
    nsv4905098copy number variation1nstd200human GRCh38 chrX: 1,908,052-2,443,863 , GRCh37.p13 chrX: 2,026,945-2,361,904 DHRSX
    nsv4968580copy number variation1nstd200human GRCh38 chr6: 161,567,720-162,085,660 , GRCh37.p13 chr6: 161,988,752-162,506,692 PRKN
    nsv4824848copy number variation1nstd200human GRCh37 chr6: 161,988,752-162,506,690 , GRCh38.p12 chr6: 161,567,720-162,085,658 PRKN
    nsv5029264copy number variation1nstd200human GRCh38 chr21: 21,181,697-21,688,676 , GRCh37.p13 chr21: 22,554,015-23,060,996 NCAM2
    nsv4865776copy number variation1nstd200human GRCh37 chr21: 22,554,015-23,060,996 , GRCh38.p12 chr21: 21,181,697-21,688,676 NCAM2
    nsv4909222copy number variation1nstd200human GRCh38 chrX: 144,491,973-144,995,601 , GRCh37.p13 chrX: 143,573,537-144,077,121 , GRCh37.p13 chrX|NW_004070890.2: 16,367-519,994 HNRNPCP10
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