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Items: 1 to 20 of 287

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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
    nsv7092592copy number variation1nstd229human GRCh38 chrX: 87,479,962-87,707,821 , GRCh37.p13 chrX: 86,734,965-86,962,821 RPSAP15, KLHL4
    nsv7092575copy number variation1nstd229human GRCh38 chrX: 87,294,511-87,940,178 , GRCh37.p13 chrX: 86,549,514-87,195,178 RPSAP15, KLHL4, 1 more genes
    nsv7081589copy number variation1nstd229human GRCh38 chrX: 87,703,505-87,711,052 , GRCh37.p13 chrX: 86,958,505-86,966,052 RPSAP15
    nsv7081588copy number variation1nstd229human GRCh38 chrX: 87,688,303-87,706,569 , GRCh37.p13 chrX: 86,943,303-86,961,569 RPSAP15
    nsv7051815inversion1nstd229human GRCh38 chrX: 86,602,265-88,989,267 , GRCh37.p13 chrX: 85,857,268-88,244,268 KLHL4, RPSAP15, 8 more genes
    nsv7050446inversion1nstd229human GRCh38 chrX: 86,445,743-87,901,693 , GRCh37.p13 chrX: 85,700,746-87,156,693 FCF1P9, KLHL4, 4 more genes
    nsv7049509inversion1nstd229human GRCh38 chrX: 87,534,179-88,184,810 , GRCh37.p13 chrX: 86,789,182-87,439,811 KLHL4, MRPS22P1, 3 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
    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
    nsv6634090copy number variation1nstd224human GRCh37 chrX: 86,732,385-87,527,284 , GRCh38.p12 chrX: 87,477,382-88,272,283 KLHL4, MRPS22P1, 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
    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
    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
    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
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