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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137736copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,263,517-155,260,560 , GRCh38.p12 chrX: 153,998,066-156,030,895 H2AB3, GDI1, 83 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5973008copy number variation2nstd209human GRCh38 chrX: 155,996,405-155,999,604 , GRCh37.p13 chrX: 155,226,070-155,229,269 IL9R
    nsv5970755copy number variation2nstd209human GRCh38 chrX: 155,993,705-155,999,604 , GRCh37.p13 chrX: 155,223,370-155,229,269 IL9R
    nsv5970181copy number variation3nstd209human GRCh38 chrX: 155,996,730-156,006,609 , GRCh37.p13 chrX: 155,226,395-155,236,274 IL9R
    nsv5968634copy number variation3nstd209human GRCh38 chrX: 156,003,110-156,007,447 , GRCh37.p13 chrX: 155,232,775-155,237,112 IL9R
    nsv5881556copy number variation1nstd209human GRCh38 chrX: 155,999,763-156,029,758 , GRCh37.p13 chrX: 155,229,428-155,259,423 WASH6P, WASIR1, 2 more genes
    nsv5868170copy number variation1nstd209human GRCh38 chrX: 156,009,003-156,009,335 , GRCh37.p13 chrX: 155,238,668-155,239,000 IL9R
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5665408inversion1nstd207human GRCh37.p13 chrX: 154,937,871-155,260,559 , GRCh38 chrX: 155,708,210-156,030,894 AMD1P2, IL9R, 8 more genes
    nsv5622070insertion1nstd207human GRCh38 chrX: 156,009,241-156,009,241 , GRCh37.p13 chrX: 155,238,906-155,238,906 IL9R
    nsv5424596copy number variation1nstd206human GRCh38 chrX: 155,902,021-156,003,787 , GRCh37.p13 chrX: 155,131,685-155,233,452 ELOCP24, IL9R, 2 more genes
    nsv5383621copy number variation1nstd186human GRCh37 chrX: 155,238,524-155,238,939 , GRCh38.p12 chrX: 156,008,859-156,009,274 IL9R
    nsv5340621translocation1nstd200human GRCh37 chr3: 931,763-931,763 , GRCh37 chrX: 155,233,197-155,233,197 , GRCh38.p12 chr3: 890,080-890,080 , GRCh38.p12 chrX: 156,003,532-156,003,532 IL9R, LOC107986059
    nsv5335260translocation1nstd200human GRCh37 chrX: 155,174,869-155,174,869 , GRCh37 chrX: 155,239,586-155,239,586 , GRCh38.p12 chrX: 155,945,205-155,945,205 , GRCh38.p12 chrX: 156,009,921-156,009,921 IL9R
    nsv5182042mobile element insertion1nstd203human GRCh38 chrX: 155,997,537-155,997,551 , GRCh37.p13 chrX: 155,227,202-155,227,216 IL9R
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv4909307copy number variation1nstd200human GRCh38 chrX: 155,956,692-156,004,248 , GRCh37.p13 chrX: 155,186,357-155,233,913 TRPC6P1, IL9R, 1 more genes
    nsv4782452copy number variation1nstd200human GRCh37 chrX: 155,238,439-155,239,076 , GRCh38.p12 chrX: 156,008,774-156,009,411 IL9R
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
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