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Items: 1 to 20 of 290

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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
    nsv7098681copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 99,551,275-101,097,764 , GRCh38.p12 chrX: 100,296,277-101,842,792 TMEM35A, TNMD, 43 more genes
    nsv7090504copy number variation1nstd229human GRCh38 chrX: 101,588,811-101,609,022 , GRCh37.p13 chrX|NW_004070883.1: 270,486-290,697 , GRCh37.p13 chrX: 100,843,788-100,864,002 ARMCX7P
    nsv7090495copy number variation1nstd229human GRCh38 chrX: 101,459,215-101,777,913 , GRCh37.p13 chrX: 100,714,203-100,962,928 , GRCh37.p13 chrX|NW_004070883.1: 140,891-389,631 ARMCX6, LOC100533636, 10 more genes
    nsv7090477copy number variation1nstd229human GRCh38 chrX: 101,314,695-102,956,469 , GRCh37.p13 chrX: 100,569,683-102,211,397 LOC105373299, RPL21P132, 59 more genes
    nsv7057877inversion1nstd229human GRCh38 chrX: 101,583,797-102,041,654 , GRCh37.p13 chrX: 100,962,929-101,296,626 ARMCX6, ZMAT1, 12 more genes
    nsv7056355inversion1nstd229human GRCh38 chrX: 101,591,789-101,606,766 , GRCh37.p13 chrX: 100,846,766-100,861,746 , GRCh37.p13 chrX|NW_004070883.1: 273,464-288,441 ARMCX7P
    nsv7044115inversion1nstd229human GRCh38 chrX: 101,597,392-101,605,770 , GRCh37.p13 chrX|NW_004070883.1: 279,067-287,445 , GRCh37.p13 chrX: 100,852,370-100,860,750 ARMCX7P
    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
    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
    nsv6290661copy number variation1nstd102humanUncertain significance GRCh37 chrX: 99,589,130-102,138,180 , GRCh38.p12 chrX: 100,334,132-102,883,252 LOC105373299, RPL36A, 80 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
    nsv6137409copy number variation1nstd213human GRCh37 chrX: 73,710,000-151,990,001 , GRCh38.p12 chrX: 74,490,165-152,821,457 ABCB7, AGTR2, 991 more genes
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