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Items: 1 to 20 of 305

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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
    nsv7090250copy number variation1nstd229human GRCh38 chrX: 88,117,223-88,983,006 , GRCh37.p13 chrX: 87,372,224-88,238,007 CPXCR1, LOC107985653, 1 more genes
    nsv7081663copy number variation1nstd229human GRCh38 chrX: 88,967,995-89,103,972 , GRCh37.p13 chrX: 88,222,996-88,358,973 LOC107985653
    nsv7081661copy number variation1nstd229human GRCh38 chrX: 88,943,024-89,000,444 , GRCh37.p13 chrX: 88,198,025-88,255,445 LOC107985653
    nsv7081659copy number variation1nstd229human GRCh38 chrX: 88,931,098-89,120,885 , GRCh37.p13 chrX: 88,186,099-88,375,886 LOC107985653
    nsv7081657copy number variation1nstd229human GRCh38 chrX: 88,919,189-89,566,968 , GRCh37.p13 chrX: 88,174,190-88,821,967 LOC102724150, SRIP2, 1 more genes
    nsv7081656copy number variation1nstd229human GRCh38 chrX: 88,916,433-89,136,421 , GRCh37.p13 chrX: 88,171,434-88,391,421 LOC107985653
    nsv7081652copy number variation1nstd229human GRCh38 chrX: 88,841,437-89,185,866 , GRCh37.p13 chrX: 88,096,438-88,440,865 LOC107985653
    nsv7081632copy number variation1nstd229human GRCh38 chrX: 88,759,052-89,112,414 , GRCh37.p13 chrX: 88,014,053-88,367,415 LOC107985653
    nsv7053613inversion1nstd229human GRCh38 chrX: 88,983,657-88,984,669 , GRCh37.p13 chrX: 88,238,658-88,239,670 LOC107985653
    nsv7051815inversion1nstd229human GRCh38 chrX: 86,602,265-88,989,267 , GRCh37.p13 chrX: 85,857,268-88,244,268 KLHL4, RPSAP15, 8 more genes
    nsv7044698inversion1nstd229human GRCh38 chrX: 87,352,100-90,785,855 , GRCh37.p13 chrX: 86,607,103-90,040,854 UBE2V1P9, MRPS22P1, 15 more genes
    nsv6636889copy number variation1nstd102humanUncertain significance GRCh37 chrX: 87,082,472-95,826,084 , GRCh38.p12 chrX: 87,827,472-96,571,085 PABPC5-AS1, KAT7P1, 57 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
    nsv6634179copy number variation1nstd224human GRCh37 chrX: 87,730,629-88,809,234 , GRCh38.p12 chrX: 88,475,628-89,554,235 CPXCR1, LOC102724150, 3 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
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