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Items: 1 to 20 of 347

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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
    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
    nsv7078347copy number variation1nstd229human GRCh38 chrX: 108,076,201-108,078,900 , GRCh37.p13 chrX: 107,319,431-107,322,130 VSIG1
    nsv7078346copy number variation1nstd229human GRCh38 chrX: 108,075,213-108,081,276 , GRCh37.p13 chrX: 107,318,443-107,324,506 VSIG1
    nsv7078345copy number variation1nstd229human GRCh38 chrX: 108,066,031-108,066,131 , GRCh37.p13 chrX: 107,309,261-107,309,361 VSIG1
    nsv7078344copy number variation1nstd229human GRCh38 chrX: 108,049,898-108,052,364 , GRCh37.p13 chrX: 107,293,128-107,295,594 VSIG1
    nsv7078343copy number variation1nstd229human GRCh38 chrX: 108,032,232-108,032,402 , GRCh37.p13 chrX: 107,275,462-107,275,632 VSIG1
    nsv7078342copy number variation1nstd229human GRCh38 chrX: 108,025,630-108,032,216 , GRCh37.p13 chrX: 107,268,860-107,275,446 VSIG1
    nsv7078341copy number variation1nstd229human GRCh38 chrX: 108,023,201-108,032,200 , GRCh37.p13 chrX: 107,266,431-107,275,430 VSIG1
    nsv7078340copy number variation1nstd229human GRCh38 chrX: 108,019,324-108,021,424 , GRCh37.p13 chrX: 107,262,554-107,264,654 VSIG1
    nsv7054337inversion1nstd229human GRCh38 chrX: 108,057,027-108,057,047 , GRCh37.p13 chrX: 107,300,257-107,300,277 VSIG1
    nsv7052621inversion1nstd229human GRCh38 chrX: 103,826,879-110,334,422 , GRCh37.p13 chrX: 103,081,809-109,577,650 CSGALNACT2P2, LOC107985662, 82 more genes
    nsv7048909inversion1nstd229human GRCh38 chrX: 107,439,593-108,392,338 , GRCh37.p13 chrX: 106,682,823-107,635,568 LOC112267910, FRMPD3-AS1, 12 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
    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
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