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Items: 1 to 20 of 336

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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
    nsv7090552copy number variation1nstd229human GRCh38 chrX: 102,570,423-102,576,588 , GRCh37.p13 chrX: 101,825,351-101,831,516 NXF4
    nsv7090551copy number variation1nstd229human GRCh38 chrX: 102,567,983-102,865,175 , GRCh37.p13 chrX: 101,822,911-102,120,103 GPRASP1, H3P45, 18 more genes
    nsv7090550copy number variation1nstd229human GRCh38 chrX: 102,555,520-102,574,173 , GRCh37.p13 chrX: 101,810,448-101,829,101 NXF4
    nsv7090548copy number variation1nstd229human GRCh38 chrX: 102,533,020-102,550,648 , GRCh37.p13 chrX: 101,787,948-101,805,576 FOXN3P1, LOC100420162, 1 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
    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
    nsv6313128copy number variation1nstd102humanPathogenic GRCh37 chrX: 101,331,999-102,771,372 , GRCh38.p12 chrX: 102,077,027-103,516,444 GPRASP3, FOXN3P1, 47 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
    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
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