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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv429616copy number variation1nstd11human NCBI36 chr13: 19,386,212-114,093,817 , GRCh37.p13 chr13: 20,488,212-115,075,715 , GRCh38.p12 chr13: 19,914,072-114,310,240 PARP4, PARP1P1, 1314 more genes
    nsv429618copy number variation1nstd11human NCBI36 chr13: 25,236,798-113,967,827 , GRCh37.p13 chr13: 26,338,798-114,949,725 , GRCh38.p12 chr13: 25,779,197-114,184,250 PARP1P1, ALOX5AP, 1174 more genes
    nsv429615copy number variation1nstd11human NCBI36 chr11: 196,767-49,155,500 , GRCh37.p13 chr11: 206,767-49,198,924 , GRCh38.p12 chr11: 206,767-49,177,372 ACP2, ADM, 976 more genes
    nsv429559copy number variation1nstd11human NCBI36 chr11: 211,584-48,203,033 , GRCh37.p13 chr11: 221,584-48,246,457 , GRCh38.p12 chr11: 221,584-48,224,905 ACP2, ADM, 938 more genes
    nsv429550copy number variation1nstd11human NCBI36 chr11: 214,676-43,781,942 , GRCh37.p13 chr11: 224,676-43,825,366 , GRCh38.p12 chr11: 224,676-43,803,816 ADM, AP2A2, 837 more genes
    nsv429610copy number variation1nstd11human NCBI36 chr6: 110,632-42,839,093 , GRCh37.p13 chr6: 165,632-42,731,115 , GRCh38.p12 chr6: 165,632-42,763,377 ABCF1, AGER, 1322 more genes
    nsv429623copy number variation1nstd11human NCBI36 chr16: 41,263-30,461,660 , GRCh37.p13 chr16: 101,263-30,554,159 , GRCh38.p12 chr16: 51,263-30,542,838 ABAT, ABCA3, 853 more genes
    nsv429619copy number variation1nstd11human NCBI36 chr16: 54,535-11,398,508 , GRCh37.p13 chr16: 114,535-11,491,007 , GRCh38.p12 chr16: 64,537-11,397,150 ABAT, ABCA3, 397 more genes
    nsv2768204copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr16: 569,967-35,986,173 , GRCh37 chr16: 619,967-35,220,544 ABAT, ABCA3, 1043 more genes
    nsv2768219copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-20,692,745 , GRCh37 chr19: 260,911-20,875,551 ACP5, TLE5, 914 more genes
    nsv2768218copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-19,745,645 , GRCh37 chr19: 260,911-19,856,454 ACP5, TLE5, 867 more genes
    nsv2768217copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-16,062,156 , GRCh37 chr19: 260,911-16,172,966 ACP5, TLE5, 724 more genes
    nsv2768229copy-neutral loss of heterozygosity1nstd125human GRCh37 chr3: 39,873,604-53,004,620 , GRCh38.p12 chr3: 39,832,113-52,970,604 ACY1, ALAS1, 400 more genes
    nsv2768220copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 5,092,438-17,933,476 , GRCh37 chr19: 5,092,449-18,044,285 ACP5, GET3, 562 more genes
    nsv2768203copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr1: 47,200,473-54,167,957 , GRCh37 chr1: 47,666,145-54,633,630 CDKN2C, CPT2, 147 more genes
    nsv2768230copy-neutral loss of heterozygosity1nstd125human GRCh37 chr3: 46,715,645-52,852,488 , GRCh38.p12 chr3: 46,674,155-52,818,472 ACY1, ALAS1, 240 more genes
    nsv2768232copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr4: 158,719,122-164,075,078 , GRCh37 chr4: 159,640,274-164,996,230 NPY1R, NPY5R, 35 more genes
    nsv2768216copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr13: 73,851,090-79,043,551 , GRCh37 chr13: 74,425,227-79,617,686 BTF3P11, CLN5, 72 more genes
    nsv2768214copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr12: 84,704,059-89,082,002 , GRCh37 chr12: 85,097,838-89,475,779 GADD45AP1, KITLG, 38 more genes
    nsv2768205copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr16: 35,880-3,872,548 , GRCh37 chr16: 85,880-3,922,549 ABCA3, ARHGDIG, 274 more genes
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