dbVar for Gene (Select 7512) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7137063	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409	RN7SL581P, HMGB1P32, 2151 more genes
nsv7098222	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 128,674,417-129,299,630 , GRCh38.p12 chrX: 129,540,440-130,165,656	LOC105373334, ZDHHC9, 11 more genes
nsv7097988	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 128,674,417-128,975,921 , GRCh38.p12 chrX: 129,540,440-129,841,945	XPNPEP2, SASH3, 4 more genes
nsv7079023	copy number variation	1	nstd229	human		GRCh38 chrX: 129,745,275-129,755,334 , GRCh37.p13 chrX: 128,879,251-128,889,310	XPNPEP2
nsv7079022	copy number variation	1	nstd229	human		GRCh38 chrX: 129,742,137-129,749,512 , GRCh37.p13 chrX: 128,876,113-128,883,488	XPNPEP2
nsv7079021	copy number variation	1	nstd229	human		GRCh38 chrX: 129,741,153-129,743,713 , GRCh37.p13 chrX: 128,875,129-128,877,689	XPNPEP2
nsv7079019	copy number variation	1	nstd229	human		GRCh38 chrX: 129,731,294-129,744,208 , GRCh37.p13 chrX: 128,865,271-128,878,184	XPNPEP2
nsv7042777	inversion	1	nstd229	human		GRCh38 chrX: 127,009,007-134,341,039 , GRCh37.p13 chrX: 126,142,990-133,475,069	ELF4, TJAP1P1, 97 more genes
nsv6636493	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 127,753,972-129,202,285 , GRCh38.p12 chrX: 128,619,994-130,068,310	LOC107985684, UTP14A, 18 more genes
nsv6636407	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066	RN7SKP31, LOC728470, 539 more genes
nsv6634242	copy number variation	1	nstd224	human		GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895	NR0B1, ALAS2, 2154 more genes
nsv6634197	copy number variation	1	nstd224	human		GRCh37 chrX: 128,690,832-128,893,417 , GRCh38.p12 chrX: 129,556,855-129,759,441	OCRL, LOC105373334, 2 more genes
nsv6633767	copy number variation	1	nstd224	human		GRCh37 chrX: 128,819,902-128,875,978 , GRCh38.p12 chrX: 129,685,925-129,742,002	XPNPEP2
nsv6315429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066	H2AB1, GPR174, 1081 more genes
nsv6315393	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383	H2BP8, LOC101060199, 2151 more genes
nsv6315389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066	RBMX, LOC100129144, 2042 more genes
nsv6315332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066	MAGT1, TAFAZZIN, 1337 more genes
nsv6315331	copy number variation	4	nstd102	human	Pathogenic	GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895	PLAC1, PGK1P1, 2154 more genes
nsv6138075	copy number variation	1	nstd206	human		GRCh38 chrX: 129,742,271-129,742,340 , GRCh37.p13 chrX: 128,876,247-128,876,316	XPNPEP2
nsv6137629	copy number variation	1	nstd213	human		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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Items: 1 to 20 of 319

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Number of Variants: 20

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