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Items: 1 to 20 of 1172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv17561copy number variation1estd20human NCBI36 chr1: 187,971,861-188,047,092 , GRCh37.p13 chr1: 189,705,238-189,780,469 , GRCh38.p12 chr1: 189,736,108-189,811,339 LINC01701
    esv17048copy number variation1estd20human NCBI36 chr5: 104,460,808-104,531,562 , GRCh37.p13 chr5: 104,432,909-104,503,663 , GRCh38.p12 chr5: 105,097,208-105,167,962 RAB9BP1
    esv20564copy number variation21estd20human NCBI36 chr10: 37,477,659-37,535,427 , GRCh37.p13 chr10: 37,437,653-37,495,421 , GRCh38.p12 chr10: 37,148,725-37,206,493 ANKRD30A
    esv11519copy number variation3estd20human NCBI36 chr10: 51,118,892-51,175,352 , GRCh37.p13 chr10|NW_003871068.1: 361,591-418,051 , GRCh37.p13 chr10: 51,448,886-51,505,346 , GRCh38.p12 chr10: 46,090,476-46,146,936 AGAP7P
    esv11182copy number variation4estd20human NCBI36 chr1: 17,102,200-17,153,475 , GRCh37.p13 chr1: 17,229,613-17,280,888 , GRCh38.p12 chr1: 16,903,118-16,954,393 CROCC
    esv12997copy number variation3estd20human NCBI36 chr7: 141,406,103-141,441,024 , GRCh37.p13 chr7|NW_003571040.1: 201,785-236,706 , GRCh37.p13 chr7: 141,759,634-141,794,555 , GRCh38.p12 chr7|NT_187562.1: 21,714-56,635 , GRCh38.p12 chr7: 142,059,834-142,094,755 MGAM
    esv13349copy number variation10estd20human NCBI36 chr10: 81,143,827-81,174,494 , GRCh37.p13 chr10: 81,473,821-81,504,488 , GRCh38.p12 chr10: 79,714,065-79,744,732 NUTM2B-AS1
    esv12664copy number variation23estd20human NCBI36 chr2: 73,863,215-73,892,893 , GRCh37.p13 chr2: 74,009,707-74,039,385 , GRCh38.p12 chr2: 73,782,580-73,812,258 C2orf78
    esv14932copy number variation9estd20human NCBI36 chr10: 81,465,041-81,494,668 , GRCh37.p13 chr10: 81,474,847-81,504,486 , GRCh38.p12 chr10: 79,715,091-79,744,730 NUTM2B-AS1
    esv12461copy number variation6estd20human NCBI36 chr10: 88,987,160-89,016,734 , GRCh37.p13 chr10: 88,997,180-89,026,754 , GRCh38.p12 chr10: 87,237,423-87,266,997 NUTM2A-AS1
    esv13617copy number variation5estd20human NCBI36 chr12: 11,395,980-11,423,993 , GRCh37.p13 chr12: 11,504,713-11,532,726 , GRCh38.p12 chr12: 11,351,779-11,379,792 , GRCh38.p12 chr12|NT_187658.1: 546,742-572,349 PRB1
    esv21190copy number variation5estd20human NCBI36 chr1: 2,577,782-2,604,497 , GRCh37.p13 chr1: 2,587,922-2,614,637 , GRCh38.p12 chr1: 2,656,483-2,683,198 , GRCh38.p12 chr1|NT_187515.1: 219,010-243,773 TTC34
    esv15136copy number variation40estd20human NCBI36 chr10: 56,116,082-56,139,577 , GRCh37.p13 chr10: 56,446,076-56,469,571 , GRCh38.p12 chr10: 54,686,316-54,709,811 PCDH15
    esv18824copy number variation22estd20human NCBI36 chr10: 18,881,143-18,902,755 , GRCh37.p13 chr10: 18,841,137-18,862,749 , GRCh38.p12 chr10: 18,552,208-18,573,820 NSUN6
    esv13991copy number variation1estd20human NCBI36 chr6: 55,934,082-55,954,657 , GRCh37.p13 chr6: 55,826,123-55,846,698 , GRCh38.p12 chr6: 55,961,325-55,981,900 LOC107986539
    esv10869copy number variation29estd20human NCBI36 chr7: 64,219,176-64,239,264 , GRCh37.p13 chr7: 64,581,741-64,601,829 , GRCh38.p12 chr7: 65,121,363-65,141,451 INTS4P1
    esv15597copy number variation1estd20human NCBI36 chr15: 21,033,004-21,052,588 , GRCh37.p13 chr15: 23,481,563-23,501,147 , GRCh38.p12 chr15: 22,371,949-22,391,533 LOC441711
    esv10276copy number variation23estd20human NCBI36 chr7: 126,301,909-126,320,398 , GRCh37.p13 chr7: 126,514,673-126,533,162 , GRCh38.p12 chr7: 126,874,619-126,893,108 GRM8
    esv17472copy number variation1estd20human NCBI36 chr4: 49,206,870-49,225,239 , GRCh37.p13 chr4: 49,512,113-49,530,482 , GRCh38.p12 chr4: 49,510,096-49,528,465 LOC107986214
    esv10693copy number variation1estd20human NCBI36 chr10: 88,818,485-88,836,679 , GRCh37.p13 chr10: 88,828,505-88,846,699 , GRCh38.p12 chr10: 87,068,748-87,086,942 GLUD1
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