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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
    nsv6636248copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 53,731,940-63,932,866 , GRCh38.p12 chrX: 53,704,997-64,712,986 ALAS2, FGD1, 89 more genes
    nsv6636004copy number variation1nstd102humanPathogenic GRCh38 chrX: 57,537,466-65,512,709 , GRCh37.p13 chrX: 57,563,899-64,732,589 ZC4H2, ZC3H12B, 43 more genes
    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
    nsv6314421complex chromosomal rearrangement3nstd102humanUncertain significance GRCh38.p12 chr22: 31,226,472-31,226,472 , GRCh38.p12 chr22: 31,226,484-31,226,484 , GRCh38.p12 chr22: 31,226,484-31,226,484 , GRCh38.p12 chr22: 31,226,615-31,226,615 , GRCh37 chr22: 31,622,458-31,622,458 , GRCh37 chr22: 31,622,470-31,622,470 , GRCh37 chr22: 31,622,470-31,622,470 , GRCh37 chr22: 31,622,601-31,622,601 , GRCh37 chrX: 62,683,198-62,683,198 , GRCh37 chrX: 62,683,200-62,683,200 , GRCh38.p12 chrX: 63,463,318-63,463,318 , GRCh38.p12 chrX: 63,463,320-63,463,320 LIMK2, LINC01278
    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
    nsv6290370copy number variation1nstd102humanUncertain significance GRCh37 chrX: 62,670,323-63,608,849 , GRCh38.p12 chrX: 63,450,443-64,388,969 KPNA4P1, MIR1468, 11 more genes
    nsv6231423copy number variation1nstd214human GRCh38 chrX: 63,546,343-63,546,414 , GRCh37.p13 chrX|NW_004070881.1: 562,076-562,147 , GRCh37.p13 chrX: 62,766,223-62,766,294 LINC01278
    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
    nsv6137404copy number variation1nstd213human GRCh37 chrX: 61,730,000-65,000,001 , GRCh38.p12 chrX: 62,510,530-65,780,159 MSN, SHC1P1, 39 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
    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
    nsv6136792copy number variation1nstd213human GRCh37 chrX: 61,730,000-70,890,001 , GRCh38.p12 chrX: 62,510,530-71,670,151 AR, ARR3, 139 more genes
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