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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148163copy number variation1nstd102humanPathogenic GRCh38 chr1: 244,051,186-244,055,631 , GRCh37.p13 chr1: 244,214,488-244,218,933 ZBTB18
    nsv5674084copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,647,872-153,650,075 , GRCh38.p12 chrX: 154,419,533-154,421,736 TAFAZZIN
    nsv4449617copy number variation1nstd45humanPathogenic GRCh38.p12 chr1: 244,048,939-244,057,476 , GRCh37 chr1: 244,212,241-244,220,778 ZBTB18
    nsv3875926copy number variation1nstd102humanBenign GRCh37 chr3: 149,267,986-149,270,023 , GRCh38.p12 chr3: 149,550,199-149,552,236 WWTR1
    nsv7098603copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,641,545-153,648,084 , GRCh38.p12 chrX: 154,413,208-154,419,745 TAFAZZIN
    nsv7098008copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,647,862-153,649,343 , GRCh38.p12 chrX: 154,419,523-154,421,004 TAFAZZIN
    nsv4454892copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 153,640,161-153,649,363 , GRCh38.p12 chrX: 154,411,824-154,421,024 TAFAZZIN, DNASE1L1
    nsv5673981copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,639,844-153,642,537 , GRCh38.p12 chrX: 154,411,508-154,414,200 DNASE1L1, TAFAZZIN
    nsv1397944copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 153,640,181-153,641,904 , GRCh38.p12 chrX: 154,411,844-154,413,567 DNASE1L1, TAFAZZIN
    nsv6314302complex chromosomal rearrangement6nstd102humanPathogenic GRCh37 chr3: 149,332,307-149,332,307 , GRCh37 chr3: 154,453,976-154,453,976 , GRCh37 chr3: 149,332,307-149,332,307 , GRCh37 chr3: 154,453,975-154,453,975 , GRCh37 chr7: 12,374,295-12,374,295 , GRCh37 chr7: 12,374,296-12,374,296 , GRCh37 chr10: 28,823,742-28,823,742 , GRCh37 chr10: 11,940,759-11,940,759 , GRCh37 chr10: 102,794,873-102,794,873 , GRCh37 chr10: 102,794,873-102,794,873 , GRCh37 chr10: 11,940,757-11,940,757 , GRCh37 chr10: 28,823,741-28,823,741 , GRCh38.p12 chr10: 101,035,116-101,035,116 , GRCh38.p12 chr10: 28,534,812-28,534,812 , GRCh38.p12 chr10: 11,898,758-11,898,758 , GRCh38.p12 chr10: 101,035,116-101,035,116 , GRCh38.p12 chr10: 11,898,760-11,898,760 , GRCh38.p12 chr10: 28,534,813-28,534,813 , GRCh38.p12 chr3: 149,614,520-149,614,520 , GRCh38.p12 chr3: 149,614,520-149,614,520 , GRCh38.p12 chr3: 154,736,187-154,736,187 , GRCh38.p12 chr3: 154,736,186-154,736,186 , GRCh38.p12 chr7: 12,334,669-12,334,669 , GRCh38.p12 chr7: 12,334,670-12,334,670 SFXN3, VWDE, 2 more genes
    nsv4728549copy number variation1nstd102humanLikely benign GRCh37 chr1: 244,125,028-244,229,161 , GRCh38.p12 chr1: 243,961,726-244,065,859 LINC02774, LOC105373258, 2 more genes
    nsv3904162copy number variation1nstd102humanPathogenic GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754 NANOGNBP3, PRXL2CP1, 2154 more genes
    nsv3913255copy number variation2nstd102humanPathogenic NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895 NHS-AS1, DUSP21, 2154 more genes
    nsv3907094copy number variation4nstd102humanPathogenic GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065 GPR119, RN7SKP81, 2153 more genes
    nsv3878553copy number variation2nstd102humanPathogenic GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100 H2AB2, RTL3, 2152 more genes
    nsv3898149copy number variation1nstd102humanPathogenic GRCh38 chrX: 20,297-156,026,127 , NCBI36 chrX: 10,297-154,908,986 , GRCh37 chrX: 70,297-155,255,792 OR3B1P, SSX4B, 2154 more genes
    nsv3877395copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174 ARMCX2, RNA5SP505, 2154 more genes
    nsv3884935copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127 NDUFB11, VN1R110P, 2154 more genes
    nsv3903061copy number variation1nstd102humanPathogenic NCBI36 chrX: 679-154,896,026 , GRCh38 chrX: 10,679-156,013,167 , GRCh37 chrX: 60,679-155,242,832 SLC38A5, CT45A1, 2152 more genes
    nsv3885865copy number variation1nstd102humanPathogenic GRCh37 chrX: 70,297-155,246,585 , GRCh38.p12 chrX: 20,297-156,016,920 MIR1277, LOC100420247, 2152 more genes
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