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Items: 1 to 20 of 268

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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
    nsv7092429copy number variation1nstd229human GRCh38 chrX: 73,765,621-73,768,562 , GRCh37.p13 chrX: 72,985,456-72,988,397 SEPHS1P4
    nsv7092423copy number variation1nstd229human GRCh38 chrX: 73,669,580-73,905,018 , GRCh37.p13 chrX: 72,889,415-73,124,853 XIST, FXYD6P3, 3 more genes
    nsv7092385copy number variation1nstd229human GRCh38 chrX: 73,568,179-73,917,249 , GRCh37.p13 chrX: 72,788,015-73,137,084 XIST, FXYD6P3, 3 more genes
    nsv7020089inversion1nstd229human GRCh38 chrX: 73,530,622-73,796,254 , GRCh37.p13 chrX: 72,750,458-73,016,089 TSIX, MAP2K4P1, 3 more genes
    nsv7018592inversion1nstd229human GRCh38 chrX: 71,642,458-75,115,067 , GRCh37.p13 chrX: 70,862,308-74,334,902 RN7SL648P, LOC101059915, 83 more genes
    nsv6636591copy number variation1nstd102humanUncertain significance GRCh37 chrX: 72,024,935-73,087,982 , GRCh38.p12 chrX: 72,805,101-73,868,147 FAM236A, CHIC1, 22 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 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
    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
    nsv6137626copy number variation1nstd213human GRCh37 chrX: 61,730,000-73,580,001 , GRCh38.p12 chrX: 62,510,530-74,360,166 AR, ARR3, 210 more genes
    nsv6137403copy number variation1nstd213human GRCh37 chrX: 61,730,000-103,250,001 , GRCh38.p12 chrX: 62,510,530-103,995,433 ABCB7, AR, 529 more genes
    nsv6137228copy number variation1nstd213human GRCh37 chrX: 72,300,000-73,440,001 , GRCh38.p12 chrX: 73,080,161-74,220,166 CDX4, RPSAP14, 28 more genes
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