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Items: 1 to 20 of 319

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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
    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
    nsv7098599copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,001,546-154,563,736 , GRCh38.p12 chrX: 153,736,092-155,334,427 TAFAZZIN, LOC105373386, 82 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
    nsv7079941copy number variation1nstd229human GRCh38 chrX: 154,611,162-154,753,512 , GRCh37.p13 chrX|NW_003871103.3: 2,045,141-2,187,491 , GRCh37.p13 chrX: 153,839,415-153,981,787 OR3B1P, IKBKGP1, 6 more genes
    nsv7079933copy number variation1nstd229human GRCh38 chrX: 154,505,501-154,724,500 , GRCh37.p13 chrX: 153,733,832-153,952,775 , GRCh37.p13 chrX|NW_003871103.3: 1,939,480-2,158,479 FAM223B, CTAG1A, 12 more genes
    nsv7079921copy number variation1nstd229human GRCh38 chrX: 154,494,011-154,710,575 , GRCh37.p13 chrX|NW_003871103.3: 1,927,990-2,144,554 , GRCh37.p13 chrX: 153,722,357-153,938,850 G6PD, FAM223B, 13 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
    nsv7050020inversion1nstd229human GRCh38 chrX: 154,606,471-155,052,434 , GRCh37.p13 chrX: 153,834,724-154,280,709 , GRCh37.p13 chrX|NW_003871103.3: 2,040,450-2,486,413 EEF1A1P31, HMGN1P37, 20 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
    nsv7046188inversion1nstd229human GRCh38 chrX: 152,545,731-155,311,806 , GRCh37.p13 chrX: 151,734,490-154,541,118 , GRCh37.p13 chrX|NW_003871103.3: 1-2,745,785 TEX28, SSR4, 133 more genes
    nsv7042456inversion1nstd229human GRCh38 chrX: 154,553,086-155,008,344 , GRCh37.p13 chrX|NW_003871103.3: 1,987,065-2,442,323 , GRCh37.p13 chrX: 153,781,301-154,236,619 F8, OR3B1P, 23 more genes
    nsv6637094copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,613,883-155,233,731 , GRCh38.p12 chrX: 154,385,523-156,004,066 FAM3A, TAFAZZIN, 65 more genes
    nsv6636407copy number variation1nstd102humanPathogenic GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066 RN7SKP31, LOC728470, 539 more genes
    nsv6634686copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 153,560,562-153,864,851 , GRCh38.p12 chrX: 154,332,212-154,636,585 ATF4P1, ATP6AP1, 24 more genes
    nsv6634391copy number variation1nstd102humanPathogenic GRCh37 chrX: 142,401,540-155,233,731 , GRCh38.p12 chrX: 143,313,746-156,004,066 CSAG4, LOC112268308, 279 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634237copy number variation1nstd224human GRCh37 chrX: 149,422,813-154,913,173 , GRCh38.p12 chrX: 150,254,602-155,683,512 ABCD1, FLNA, 182 more genes
    nsv6315439copy number variation2nstd102humanPathogenic GRCh37 chrX: 152,372,767-155,233,731 , GRCh38.p12 chrX: 153,106,941-156,004,066 SNORA36A, VBP1, 126 more genes
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