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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
    nsv7098918copy number variation1nstd102humanUncertain significance GRCh38 chrX: 153,151,471-153,250,484 , GRCh37.p13 chrX|NW_003871103.3: 585,454-684,467 , GRCh37.p13 chrX: 152,248,403-152,513,928 LOC105373373, MAGEA1
    nsv7098869copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,586,015-154,774,957 , GRCh38.p12 chrX: 140,503,850-155,545,296 MAGEA6, LOC101928832, 303 more genes
    nsv7098598copy number variation2nstd102humanUncertain significance GRCh37 chrX: 152,014,869-153,363,122 , GRCh38.p12 chrX: 152,846,325-154,097,665 AVPR2, HMGN2P48, 56 more genes
    nsv7097996copy number variation6nstd102humanPathogenic GRCh37 chrX: 152,014,869-155,171,615 , GRCh38.p12 chrX: 152,846,325-155,941,951 PHF10P1, ZNF185, 132 more genes
    nsv7097995copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 152,014,869-154,563,736 , GRCh38.p12 chrX: 152,846,325-155,334,427 RN7SL697P, CYCSP45, 118 more genes
    nsv7085488copy number variation1nstd229human GRCh38 chrX: 153,183,861-153,184,037 , GRCh37.p13 chrX: 152,481,363-152,481,539 , GRCh37.p13 chrX|NW_003871103.3: 617,844-618,020 MAGEA1
    nsv7085487copy number variation1nstd229human GRCh38 chrX: 153,179,979-153,180,029 , GRCh37.p13 chrX: 152,485,371-152,485,421 , GRCh37.p13 chrX|NW_003871103.3: 613,962-614,012 MAGEA1
    nsv7085485copy number variation1nstd229human GRCh38 chrX: 153,172,350-153,179,017 , GRCh37.p13 chrX|NW_003871103.3: 606,333-613,000 , GRCh37.p13 chrX: 152,486,383-152,493,052 MAGEA1
    nsv7085484copy number variation1nstd229human GRCh38 chrX: 153,171,204-153,182,615 , GRCh37.p13 chrX|NW_003871103.3: 605,187-616,598 , GRCh37.p13 chrX: 152,482,785-152,494,198 MAGEA1
    nsv7085479copy number variation1nstd229human GRCh38 chrX: 153,093,215-153,204,043 , GRCh37.p13 chrX|NW_003871103.3: 527,198-638,026 , GRCh37.p13 chrX: 152,274,971-152,541,733 MAGEA1, LOC728307
    nsv7085477copy number variation1nstd229human GRCh38 chrX: 153,075,549-153,179,115 , GRCh37.p13 chrX|NW_003871103.3: 509,532-613,098 MAGEA1, PNMA6B, 1 more genes
    nsv7085476copy number variation1nstd229human GRCh38 chrX: 153,075,484-153,238,268 , GRCh37.p13 chrX|NW_003871103.3: 509,467-672,251 PNMA6B, LOC728307, 3 more genes
    nsv7079704copy number variation1nstd229human GRCh38 chrX: 152,941,694-153,188,100 , GRCh37.p13 chrX|NW_003871103.3: 375,677-622,083 ZNF185, PNMA6B, 7 more genes
    nsv7057928inversion1nstd229human GRCh38 chrX: 152,528,769-155,098,506 , GRCh37.p13 chrX: 151,734,490-154,326,781 , GRCh37.p13 chrX|NW_003871103.3: 1-2,532,485 F8, ATP6AP1, 128 more genes
    nsv7054515inversion1nstd229human GRCh38 chrX: 152,922,716-153,299,326 , GRCh37.p13 chrX|NW_003871103.3: 356,699-733,309 HMGN2P48, LOC112268308, 10 more genes
    nsv7050000inversion1nstd229human GRCh38 chrX: 153,164,176-153,183,158 , GRCh37.p13 chrX|NW_003871103.3: 598,159-617,141 , GRCh37.p13 chrX: 152,482,242-152,501,222 MAGEA1
    nsv7049994inversion1nstd229human GRCh38 chrX: 152,895,318-153,240,335 , GRCh37.p13 chrX|NW_003871103.3: 329,301-674,318 LOC112268308, HMGN2P48, 9 more genes
    nsv7046652inversion1nstd229human GRCh38 chrX: 153,102,084-153,299,419 , GRCh37.p13 chrX|NW_003871103.3: 536,067-733,402 MAGEA1, LOC728307, 2 more genes
    nsv7046320inversion1nstd229human GRCh38 chrX: 152,800,888-155,032,704 , GRCh37.p13 chrX|NW_003871103.3: 234,871-2,466,683 , GRCh37.p13 chrX: 151,969,427-154,260,979 FUNDC2, PNCK, 111 more genes
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