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Items: 1 to 20 of 274

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7089282copy number variation1nstd229human GRCh38 chrX: 78,744,901-78,754,300 , GRCh37.p13 chrX: 78,000,398-78,009,797 LPAR4
    nsv7089281copy number variation1nstd229human GRCh38 chrX: 78,744,753-78,748,528 , GRCh37.p13 chrX: 78,000,250-78,004,025 LPAR4
    nsv7089271copy number variation1nstd229human GRCh38 chrX: 78,587,809-78,845,742 , GRCh37.p13 chrX: 77,843,306-78,101,239 PPATP2, RPL7P54, 3 more genes
    nsv7026063inversion1nstd229human GRCh38 chrX: 76,257,068-80,095,987 , GRCh37.p13 chrX: 75,477,467-77,450,502 ATRX, MAGEE1, 40 more genes
    nsv7018633inversion1nstd229human GRCh38 chrX: 76,256,859-80,096,106 , GRCh37.p13 chrX: 75,477,258-77,450,502 LDHBP2, ATP7A, 40 more genes
    nsv6636302copy number variation1nstd102humanUncertain significance GRCh37 chrX: 77,544,318-78,390,511 , GRCh38.p12 chrX: 78,288,821-79,135,014 HMGN1P34, CYSLTR1, 9 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
    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
    nsv6313464copy number variation1nstd102humanUncertain significance GRCh37 chrX: 72,095,006-88,455,505 , GRCh38.p12 chrX: 72,875,172-89,200,506 LOC105373285, LOC105373288, 170 more genes
    nsv6313346copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,974,855-79,123,671 , GRCh38.p12 chrX: 62,755,385-79,868,171 RPS7P14, RNY4P23, 280 more genes
    nsv6313230copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,877,278-79,123,671 , GRCh38.p12 chrX: 62,657,808-79,868,171 SSBL2P, LOC105373239, 280 more genes
    nsv6137634copy number variation1nstd213human GRCh37 chrX: 78,010,000-78,720,001 , GRCh38.p12 chrX: 78,754,503-79,464,504 LPAR4, ITM2A, 9 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
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