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Items: 1 to 20 of 308

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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
    nsv7098489copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,858,121-107,979,574 , GRCh38.p12 chrX: 108,614,891-108,736,344 IRS4-AS1, IRS4, 1 more genes
    nsv7098213copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,898,541-107,979,574 , GRCh38.p12 chrX: 108,655,311-108,736,344 COL4A5, IRS4, 1 more genes
    nsv7098107copy number variation1nstd102humanPathogenic GRCh37 chrX: 106,046,084-108,868,249 , GRCh38.p12 chrX: 106,802,854-109,625,020 VSIG1, NXT2, 32 more genes
    nsv7078383copy number variation1nstd229human GRCh38 chrX: 108,697,312-108,720,174 , GRCh37.p13 chrX: 107,940,542-107,963,404 IRS4, COL4A5
    nsv7052621inversion1nstd229human GRCh38 chrX: 103,826,879-110,334,422 , GRCh37.p13 chrX: 103,081,809-109,577,650 CSGALNACT2P2, LOC107985662, 82 more genes
    nsv7044993inversion1nstd229human GRCh38 chrX: 104,618,913-113,302,073 , GRCh37.p13 chrX: 103,863,594-112,545,300 NCBP2L, TEX13B, 92 more genes
    nsv7041719inversion1nstd229human GRCh38 chrX: 105,592,744-110,464,662 , GRCh37.p13 chrX: 104,836,737-109,707,890 LOC105373312, PPP6CP, 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
    nsv6633565copy number variation1nstd224human GRCh37 chrX: 107,804,808-114,879,367 , GRCh38.p12 chrX: 108,561,578-115,645,047 DCX, IL13RA2, 80 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
    nsv6313304copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,782,956-107,979,574 , GRCh38.p12 chrX: 108,539,726-108,736,344 IRS4-AS1, IRS4, 1 more genes
    nsv6313301copy number variation1nstd102humanPathogenic GRCh37 chrX: 101,982,475-116,885,339 , GRCh38.p12 chrX: 102,727,547-117,751,376 TMSB15B, GLUD1P9, 207 more genes
    nsv6313131copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,849,932-107,979,574 , GRCh38.p12 chrX: 108,606,702-108,736,344 IRS4, COL4A5, 1 more genes
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