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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 AGT, MAP10, 221 more genes
    nsv7139950insertion1nstd232human GRCh37.p13 chr1: 235,323,962-235,323,962 , GRCh38.p12 chr1: 235,160,647-235,160,647 RBM34
    nsv7137173copy number variation1nstd102humanPathogenic GRCh38 chr1: 233,502,994-236,105,019 , GRCh37.p13 chr1: 233,638,740-236,268,319 ARID4B, MTND3P8, 58 more genes
    nsv7099266copy number variation1nstd231human GRCh38.p12 chr1: 226,993,371-235,936,592 , GRCh37 chr1: 227,181,072-236,099,892 ACTA1, AGT, 223 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv7048010inversion1nstd229human GRCh38 chr1: 233,396,223-235,667,657 , GRCh37.p13 chr1: 233,531,969-235,830,957 RN7SL668P, LINC02961, 52 more genes
    nsv7044547inversion1nstd229human GRCh38 chr1: 234,053,817-240,091,334 , GRCh37.p13 chr1: 234,189,563-240,254,634 RNU6-725P, RNU6-968P, 101 more genes
    nsv7044310inversion1nstd229human GRCh38 chr1: 230,890,958-235,370,433 , GRCh37.p13 chr1: 231,026,704-235,533,748 TARBP1, LOC105373170, 86 more genes
    nsv6676611copy number variation1nstd229human GRCh38 chr1: 235,148,664-235,157,114 , GRCh37.p13 chr1: 235,311,979-235,320,429 RBM34
    nsv6674675copy number variation1nstd229human GRCh38 chr1: 235,153,388-235,156,795 , GRCh37.p13 chr1: 235,316,703-235,320,110 RBM34
    nsv6668767copy number variation1nstd229human GRCh38 chr1: 235,146,733-235,151,679 , GRCh37.p13 chr1: 235,310,048-235,314,994 RBM34
    nsv6668066copy number variation1nstd229human GRCh38 chr1: 235,144,105-235,146,245 , GRCh37.p13 chr1: 235,307,420-235,309,560 RBM34
    nsv6665328copy number variation1nstd229human GRCh38 chr1: 235,132,781-235,650,007 , GRCh37.p13 chr1: 235,296,096-235,813,307 MTND4LP21, LOC100418822, 16 more genes
    nsv6665048copy number variation1nstd229human GRCh38 chr1: 235,161,107-235,164,517 , GRCh37.p13 chr1: 235,324,422-235,327,832 RBM34
    nsv6664080copy number variation1nstd229human GRCh38 chr1: 235,142,365-235,148,887 , GRCh37.p13 chr1: 235,305,680-235,312,202 RBM34
    nsv6663454copy number variation1nstd229human GRCh38 chr1: 235,161,068-235,161,173 , GRCh37.p13 chr1: 235,324,383-235,324,488 RBM34
    nsv6660567copy number variation1nstd229human GRCh38 chr1: 234,838,301-235,712,200 , GRCh37.p13 chr1: 234,974,048-235,875,500 LYST, SNORA14B, 25 more genes
    nsv6637109copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,895,447-238,787,061 , GRCh38.p12 chr1: 232,759,701-238,623,761 RPL9P10, LOC105373207, 105 more genes
    nsv6637037copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,827,966-240,750,334 , GRCh38.p12 chr1: 232,692,220-240,587,034 RNU1-74P, EDARADD, 123 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
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