HGDP01223 AND nstd30 - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv470095	copy number variation	1	nstd30	human		NCBI36 chr4: 179,318,010-179,411,162 , GRCh37.p13 chr4: 179,081,016-179,174,168 , GRCh38.p12 chr4: 178,159,862-178,253,014	LOC105377562
nsv470830	copy number variation	2	nstd30	human		NCBI36 chr6: 67,613,966-67,685,128 , GRCh37.p13 chr6: 67,557,245-67,628,407 , GRCh38.p12 chr6: 66,847,352-66,918,514	LOC107986540
nsv470433	copy number variation	34	nstd30	human		NCBI36 chr18: 64,892,426-64,906,488 , GRCh37.p13 chr18: 66,741,446-66,755,508 , GRCh38.p12 chr18: 69,074,209-69,088,271	CCDC102B
nsv470808	copy number variation	11	nstd30	human		NCBI36 chr6: 31,463,297-31,470,909 , GRCh37.p13 chr6\|NT_167249.1: 2,689,103-2,696,721 , GRCh37.p13 chr6\|NT_167246.1: 2,701,768-2,709,373 , GRCh37.p13 chr6: 31,355,318-31,362,930 , GRCh38.p12 chr6: 31,387,541-31,395,153 , GRCh38.p12 chr6\|NT_167249.2: 2,689,805-2,697,423	MICA-AS1
nsv470005	copy number variation	1	nstd30	human		NCBI36 chr4: 6,123,823-6,164,460 , GRCh37.p13 chr4: 6,072,922-6,113,559 , GRCh38.p12 chr4: 6,071,195-6,111,832	JAKMIP1
nsv470073	copy number variation	4	nstd30	human		NCBI36 chr4: 133,121,505-133,320,544 , GRCh37.p13 chr4: 132,902,055-133,101,094 , GRCh38.p12 chr4: 131,980,900-132,179,939	LOC105377428,
nsv470509	copy number variation	2	nstd30	human		NCBI36 chr2: 194,884,458-195,024,254 , GRCh37.p13 chr2: 195,176,213-195,316,009 , GRCh38.p12 chr2: 194,311,489-194,451,285	LINC01821, LOC105373816
nsv471093	copy number variation	2	nstd30	human		NCBI36 chr3: 176,552,882-176,585,032 , GRCh37.p13 chr3: 175,070,188-175,102,338 , GRCh38.p12 chr3: 175,352,399-175,384,549 , GRCh38.p12 chr3\|NW_019805489.1: 19,190-58,065	NAALADL2, MIR4789
nsv470148	copy number variation	1	nstd30	human		GRCh38.p12 chr19: 48,865,586-48,906,934 , GRCh37.p13 chr19: 49,368,843-49,410,191 , NCBI36 chr19: 54,060,655-54,102,003	NUCB1, TULP2, 2 more genes
nsv469958	copy number variation	54	nstd30	human		NCBI36 chr11: 55,127,596-55,352,889 , GRCh37.p13 chr11: 55,371,020-55,596,313 , GRCh38.p12 chr11: 55,603,544-55,828,837	OR5D3P, OR5D2P, 13 more genes
nsv470029	copy number variation	1	nstd30	human		NCBI36 chr4: 35,244,357-35,353,304 , GRCh37.p13 chr4: 35,567,962-35,676,909 , GRCh38.p12 chr4: 35,566,340-35,675,287	0
nsv470782	copy number variation	1	nstd30	human		NCBI36 chr1: 236,824,683-236,846,513 , GRCh37.p13 chr1: 238,758,060-238,779,890 , GRCh38.p12 chr1: 238,594,760-238,616,590	0
nsv470711	copy number variation	1	nstd30	human		NCBI36 chr1: 46,432,882-46,583,117 , GRCh38.p12 chr1: 46,194,623-46,344,858 , GRCh37.p13 chr1: 46,660,295-46,810,530	UQCRH, RAD54L, 5 more genes
nsv470528	copy number variation	1	nstd30	human		GRCh38.p12 chr2: 239,513,740-239,545,860 , NCBI36 chr2: 240,100,371-240,132,491 , GRCh37.p13 chr2: 240,435,434-240,467,554	0

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