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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054851inversion1nstd229human GRCh38 chr2: 112,725,002-112,728,283 , GRCh37.p13 chr2: 113,482,579-113,485,860 NT5DC4
    nsv7044064inversion1nstd229human GRCh38 chr2: 112,019,946-120,004,832 , GRCh37.p13 chr2: 112,777,523-120,762,408 LOC105373563, IL1A, 112 more genes
    nsv7042586inversion1nstd229human GRCh38 chr2: 111,572,275-118,829,502 , GRCh37.p13 chr2: 112,329,852-119,587,078 LOC105373579, NT5DC4, 103 more genes
    nsv6696164copy number variation1nstd229human GRCh38 chr2: 112,740,109-112,740,161 , GRCh37.p13 chr2: 113,497,686-113,497,738 CKAP2L, NT5DC4
    nsv6692799copy number variation1nstd229human GRCh38 chr2: 112,728,073-112,738,258 , GRCh37.p13 chr2: 113,485,650-113,495,835 NT5DC4, CKAP2L
    nsv6688618copy number variation1nstd229human GRCh38 chr2: 112,717,666-112,720,754 , GRCh37.p13 chr2: 113,475,243-113,478,331 NT5DC4
    nsv6686734copy number variation1nstd229human GRCh38 chr2: 112,726,139-112,736,942 , GRCh37.p13 chr2: 113,483,716-113,494,519 CKAP2L, NT5DC4
    nsv6685169copy number variation1nstd229human GRCh38 chr2: 112,712,975-112,732,229 , GRCh37.p13 chr2: 113,470,552-113,489,806 NT5DC4
    nsv6681382copy number variation1nstd229human GRCh38 chr2: 112,715,737-112,719,809 , GRCh37.p13 chr2: 113,473,314-113,477,386 NT5DC4
    nsv6352306copy number variation1nstd223human GRCh38 chr2: 112,726,138-112,736,943 , GRCh37.p13 chr2: 113,483,715-113,494,520 CKAP2L, NT5DC4
    nsv6350915copy number variation1nstd223human GRCh38 chr2: 112,719,731-112,720,311 , GRCh37.p13 chr2: 113,477,308-113,477,888 NT5DC4
    nsv6339234copy number variation1nstd223human GRCh38 chr2: 112,715,737-112,719,809 , GRCh37.p13 chr2: 113,473,314-113,477,386 NT5DC4
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314748copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432 MED15P9, TMEM37, 474 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313770copy number variation1nstd102humanPathogenic GRCh37 chr2: 113,188,197-128,144,700 , GRCh38.p12 chr2: 112,430,620-127,387,124 LOC105373575, RPS20P11, 174 more genes
    nsv6291353copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036 LINC01120, LOC105373585, 490 more genes
    nsv6291237copy number variation1nstd102humanUncertain significance GRCh37 chr2: 113,295,194-114,085,649 , GRCh38.p12 chr2: 112,537,617-113,328,072 CKAP2L, LOC105373567, 30 more genes
    nsv6056542insertion1nstd212human GRCh38 chr2: 112,732,491-112,732,491 , GRCh37.p13 chr2: 113,490,068-113,490,068 NT5DC4
    nsv6053503insertion1nstd212human GRCh38 chr2: 112,732,378-112,732,378 , GRCh37.p13 chr2: 113,489,955-113,489,955 NT5DC4
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