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Items: 1 to 20 of 340

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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
    nsv7083281copy number variation1nstd229human GRCh38 chrX: 120,804,233-121,118,844 , GRCh37.p13 chrX: 119,938,087-120,252,698 CT47B1, PA2G4P1, 15 more genes
    nsv7083259copy number variation1nstd229human GRCh38 chrX: 120,554,910-121,054,983 , GRCh37.p13 chrX: 119,688,765-120,188,837 CT47A1, C1GALT1C1, 20 more genes
    nsv7057233inversion1nstd229human GRCh38 chrX: 117,599,215-122,918,174 , GRCh37.p13 chrX: 116,733,178-122,052,027 NUDT19P1, RHOXF1P2, 89 more genes
    nsv7049773inversion1nstd229human GRCh38 chrX: 118,660,648-122,841,710 , GRCh37.p13 chrX: 117,794,611-121,975,563 NUDT19P6, MRPS17P9, 83 more genes
    nsv7038305inversion1nstd229human GRCh38 chrX: 118,464,002-122,855,541 , GRCh37.p13 chrX: 117,597,965-121,989,394 UBE2V1P16, RNY3P16, 84 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
    nsv6137583copy number variation1nstd213human GRCh37 chrX: 119,960,000-120,240,001 , GRCh38.p12 chrX: 120,826,146-121,106,147 GLUD2, CT47A11, 15 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
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