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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7088481copy number variation1nstd229human GRCh38 chrX: 69,205,632-69,205,703 , GRCh37.p13 chrX: 68,425,475-68,425,546 LINC00269
    nsv7088480copy number variation1nstd229human GRCh38 chrX: 69,201,701-69,306,800 , GRCh37.p13 chrX: 68,421,544-68,526,643 LINC00269
    nsv7088479copy number variation1nstd229human GRCh38 chrX: 69,182,526-69,186,002 , GRCh37.p13 chrX: 68,402,369-68,405,845 LINC00269
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
    nsv6315332copy number variation1nstd102humanPathogenic GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066 MAGT1, TAFAZZIN, 1337 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6313346copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,974,855-79,123,671 , GRCh38.p12 chrX: 62,755,385-79,868,171 RPS7P14, RNY4P23, 280 more genes
    nsv6313230copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,877,278-79,123,671 , GRCh38.p12 chrX: 62,657,808-79,868,171 SSBL2P, LOC105373239, 280 more genes
    nsv6290468copy number variation1nstd102humanUncertain significance GRCh37 chrX: 67,968,923-68,529,063 , GRCh38.p12 chrX: 68,749,081-69,309,220 LOC102723911, LOC107985646, 7 more genes
    nsv6137630copy number variation1nstd213human GRCh37 chrX: 68,250,000-68,790,001 , GRCh38.p12 chrX: 69,030,157-69,570,158 NALF2, PJA1, 6 more genes
    nsv6137629copy number variation1nstd213human GRCh37 chrX: 66,030,000-152,230,001 , GRCh38.p12 chrX: 66,810,158-153,061,271 ABCB7, AGTR2, 1162 more genes
    nsv6137626copy number variation1nstd213human GRCh37 chrX: 61,730,000-73,580,001 , GRCh38.p12 chrX: 62,510,530-74,360,166 AR, ARR3, 210 more genes
    nsv6137403copy number variation1nstd213human GRCh37 chrX: 61,730,000-103,250,001 , GRCh38.p12 chrX: 62,510,530-103,995,433 ABCB7, AR, 529 more genes
    nsv6137221copy number variation1nstd213human GRCh37 chrX: 66,020,000-152,230,001 , GRCh38.p12 chrX: 66,800,158-153,061,271 ABCB7, AGTR2, 1162 more genes
    nsv6137215copy number variation3nstd213human GRCh37 chrX: 61,730,000-152,230,001 , GRCh38.p12 chrX: 62,510,530-153,061,271 ABCB7, AGTR2, 1217 more genes
    nsv6137213copy number variation1nstd213human GRCh37 chrX: 52,570,000-152,220,001 , GRCh38.p12 chrX: 52,729,004-152,738,707 ABCB7, ACTG1P10, 1298 more genes
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