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Items: 1 to 20 of 271

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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
    nsv7091024copy number variation1nstd229human GRCh38 chrX: 126,539,609-126,559,834 , GRCh37.p13 chrX: 125,673,592-125,693,817 DCAF12L1
    nsv7091023copy number variation1nstd229human GRCh38 chrX: 126,528,007-126,938,885 , GRCh37.p13 chrX: 125,661,990-126,072,868 PRR32, MTCYBP38, 1 more genes
    nsv6636407copy number variation1nstd102humanPathogenic GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066 RN7SKP31, LOC728470, 539 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
    nsv6290546copy number variation1nstd102humanPathogenic GRCh37 chrX: 119,173,583-126,584,360 , GRCh38.p12 chrX: 120,039,618-127,450,379 FBLIM1P1, PNPLA10P, 81 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
    nsv6137579copy number variation1nstd213human GRCh37 chrX: 114,940,000-134,860,001 , GRCh38.p12 chrX: 115,705,680-135,719,285 AGTR2, SLC25A5, 295 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
    nsv6137362copy number variation1nstd213human GRCh37 chrX: 104,480,000-134,870,001 , GRCh38.p12 chrX: 105,235,316-135,719,285 AGTR2, SLC25A5, 423 more genes
    nsv6137221copy number variation1nstd213human GRCh37 chrX: 66,020,000-152,230,001 , GRCh38.p12 chrX: 66,800,158-153,061,271 ABCB7, AGTR2, 1162 more genes
    nsv6137215copy number variation3nstd213human GRCh37 chrX: 61,730,000-152,230,001 , GRCh38.p12 chrX: 62,510,530-153,061,271 ABCB7, AGTR2, 1217 more genes
    nsv6137213copy number variation1nstd213human GRCh37 chrX: 52,570,000-152,220,001 , GRCh38.p12 chrX: 52,729,004-152,738,707 ABCB7, ACTG1P10, 1298 more genes
    nsv6136960copy number variation1nstd213human GRCh37 chrX: 103,300,000-150,710,001 , GRCh38.p12 chrX: 104,045,432-151,541,529 AGTR2, SLC25A5, 642 more genes
    nsv6136791copy number variation1nstd213human GRCh37 chrX: 61,730,000-134,860,001 , GRCh38.p12 chrX: 62,510,530-135,719,285 ABCB7, AGTR2, 967 more genes
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