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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098217copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 117,629,935-119,761,021 , GRCh38.p12 chrX: 118,495,972-120,627,166 HNRNPA1P28, RNU7-86P, 59 more genes
    nsv7083023copy number variation1nstd229human GRCh38 chrX: 118,748,493-118,748,701 , GRCh37.p13 chrX: 117,882,456-117,882,664 IL13RA1
    nsv7083013copy number variation1nstd229human GRCh38 chrX: 118,530,673-119,150,659 , GRCh37.p13 chrX: 117,664,636-118,284,622 TMEM30BP1, COBLP1, 9 more genes
    nsv7057233inversion1nstd229human GRCh38 chrX: 117,599,215-122,918,174 , GRCh37.p13 chrX: 116,733,178-122,052,027 NUDT19P1, RHOXF1P2, 89 more genes
    nsv7055271inversion1nstd229human GRCh38 chrX: 114,091,775-119,749,531 , GRCh37.p13 chrX: 115,732,291-118,883,494 ZCCHC12, CT47C1, 83 more genes
    nsv7053216inversion1nstd229human GRCh38 chrX: 114,054,506-118,815,100 , GRCh37.p13 chrX: 113,297,697-115,918,761 LUZP4, LOC107985681, 57 more genes
    nsv7049773inversion1nstd229human GRCh38 chrX: 118,660,648-122,841,710 , GRCh37.p13 chrX: 117,794,611-121,975,563 NUDT19P6, MRPS17P9, 83 more genes
    nsv7048914inversion1nstd229human GRCh38 chrX: 113,754,776-118,814,265 , GRCh37.p13 chrX: 112,998,052-115,918,761 RN7SL712P, SLC6A14, 61 more genes
    nsv7048750inversion1nstd229human GRCh38 chrX: 114,054,489-118,815,074 , GRCh37.p13 chrX: 113,297,680-115,918,761 CT83, MIR1912, 57 more genes
    nsv7041242inversion1nstd229human GRCh38 chrX: 118,462,388-118,831,142 , GRCh37.p13 chrX: 117,596,351-117,965,105 IL13RA1, RBBP8P1, 3 more genes
    nsv7038305inversion1nstd229human GRCh38 chrX: 118,464,002-122,855,541 , GRCh37.p13 chrX: 117,597,965-121,989,394 UBE2V1P16, RNY3P16, 84 more genes
    nsv6637078copy number variation1nstd102humanUncertain significance GRCh37 chrX: 117,651,370-118,792,490 , GRCh38.p12 chrX: 118,517,407-119,658,527 LONRF3, CT47C1, 28 more genes
    nsv6636543copy number variation1nstd102humanPathogenic GRCh37 chrX: 93,805,850-118,913,329 , GRCh38.p12 chrX: 94,550,851-119,779,366 TRPC5OS, LOC105373314, 351 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634192copy number variation1nstd224human GRCh37 chrX: 117,762,197-117,989,626 , GRCh38.p12 chrX: 118,628,234-118,855,663 IL13RA1, DOCK11, 4 more genes
    nsv6315429copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066 H2AB1, GPR174, 1081 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
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