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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
    nsv7092966copy number variation1nstd229human GRCh38 chrX: 94,283,314-96,950,909 , GRCh37.p13 chrX: 93,538,313-96,205,908 LOC105373294, RPS7P13, 24 more genes
    nsv7092691copy number variation1nstd229human GRCh38 chrX: 90,583,822-99,472,797 , GRCh37.p13 chrX: 89,838,821-98,727,795 RNU2-26P, KRT18P11, 57 more genes
    nsv7081963copy number variation1nstd229human GRCh38 chrX: 96,827,069-96,977,680 , GRCh37.p13 chrX: 96,082,068-96,232,679 RPA4, NDUFB5P2, 1 more genes
    nsv7052177inversion1nstd229human GRCh38 chrX: 96,056,744-98,308,879 , GRCh37.p13 chrX: 95,311,743-97,563,877 RPS29P28, NDUFB5P2, 15 more genes
    nsv7047882inversion1nstd229human GRCh38 chrX: 96,054,797-100,053,452 , GRCh37.p13 chrX: 95,309,796-99,308,450 RPL6P29, LOC101928508, 20 more genes
    nsv7046571inversion1nstd229human GRCh38 chrX: 96,741,488-97,115,665 , GRCh37.p13 chrX: 95,996,487-96,370,664 DIAPH2, RPA4, 1 more genes
    nsv7041190inversion1nstd229human GRCh38 chrX: 94,312,916-96,897,649 , GRCh37.p13 chrX: 93,567,915-96,152,648 CALM1P1, KAT7P1, 24 more genes
    nsv6636543copy number variation1nstd102humanPathogenic GRCh37 chrX: 93,805,850-118,913,329 , GRCh38.p12 chrX: 94,550,851-119,779,366 TRPC5OS, LOC105373314, 351 more genes
    nsv6634400copy number variation1nstd102humanPathogenic GRCh37 chrX: 90,868,186-99,828,437 , GRCh38.p12 chrX: 91,613,187-100,573,440 LOC100420872, LOC100420955, 55 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315429copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066 H2AB1, GPR174, 1081 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
    nsv6290213copy number variation1nstd102humanPathogenic GRCh37 chrX: 88,361,395-99,758,442 , GRCh38.p12 chrX: 89,106,394-100,503,445 LOC107985647, CCNB1IP1P3, 70 more genes
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 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
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